Can a cyclic Amine for a Amide?
$begingroup$
This is a question from CAIE!
I need to understand why the secondary amine in serotonin molecule doesnot undergo condensation reaction with $CH_3COCl$ ?
because as far as I know, there should be an amide formation for this reaction.
Here's a picture of Serotonin:
I must be lacking some information making that $NH$ unsuitable for this reaction. And I know that the other amine and the phenol reacts with $CH_3COCl$.
organic-chemistry amines amides
asked 4 hours ago
Amar30657Amar30657
626
$endgroup$
|
show 2 more comments
$begingroup$
This is a question from CAIE!
I need to understand why the secondary amine in serotonin molecule doesnot undergo condensation reaction with $CH_3COCl$ ?
because as far as I know, there should be an amide formation for this reaction.
Here's a picture of Serotonin:
I must be lacking some information making that $NH$ unsuitable for this reaction. And I know that the other amine and the phenol reacts with $CH_3COCl$.
organic-chemistry amines amides
asked 4 hours ago
Amar30657Amar30657
626
$endgroup$
$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
1
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
1
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago
|
show 2 more comments
$begingroup$
This is a question from CAIE!
I need to understand why the secondary amine in serotonin molecule doesnot undergo condensation reaction with $CH_3COCl$ ?
because as far as I know, there should be an amide formation for this reaction.
Here's a picture of Serotonin:
I must be lacking some information making that $NH$ unsuitable for this reaction. And I know that the other amine and the phenol reacts with $CH_3COCl$.
organic-chemistry amines amides
asked 4 hours ago
Amar30657Amar30657
626
$endgroup$
This is a question from CAIE!
I need to understand why the secondary amine in serotonin molecule doesnot undergo condensation reaction with $CH_3COCl$ ?
because as far as I know, there should be an amide formation for this reaction.
Here's a picture of Serotonin:
I must be lacking some information making that $NH$ unsuitable for this reaction. And I know that the other amine and the phenol reacts with $CH_3COCl$.
organic-chemistry amines amides
organic-chemistry amines amides
asked 4 hours ago
Amar30657Amar30657
626
asked 4 hours ago
Amar30657Amar30657
626
asked 4 hours ago
Amar30657Amar30657
626
asked 4 hours ago
Amar30657Amar30657
626
asked 4 hours ago
Amar30657Amar30657
626
626
$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
1
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
1
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago
|
show 2 more comments
$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
1
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
1
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago
$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
1
1
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
1
1
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago
|
show 2 more comments
1 Answer
1
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$begingroup$
The heterocycle in this question is indole and is aromatic. This means that the N lone pair is delocalised and not readily available for nucleophilic attack. Think of it as similar in reactivity to a secondary amide nitrogen RCONHR. Generally you need to formally deprotonate to functionalise though there are some interesting techniques using carbonyl azoles catalysed by DBU reference and others using aldehyde and alcohol substrates such as here. Note that 3-unsubstituted indoles react with acyl halides by F-C acylation at the 3 position example
answered 1 hour ago
WaylanderWaylander
7,04811424
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1 Answer
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$begingroup$
The heterocycle in this question is indole and is aromatic. This means that the N lone pair is delocalised and not readily available for nucleophilic attack. Think of it as similar in reactivity to a secondary amide nitrogen RCONHR. Generally you need to formally deprotonate to functionalise though there are some interesting techniques using carbonyl azoles catalysed by DBU reference and others using aldehyde and alcohol substrates such as here. Note that 3-unsubstituted indoles react with acyl halides by F-C acylation at the 3 position example
answered 1 hour ago
WaylanderWaylander
7,04811424
$endgroup$
add a comment |
$begingroup$
The heterocycle in this question is indole and is aromatic. This means that the N lone pair is delocalised and not readily available for nucleophilic attack. Think of it as similar in reactivity to a secondary amide nitrogen RCONHR. Generally you need to formally deprotonate to functionalise though there are some interesting techniques using carbonyl azoles catalysed by DBU reference and others using aldehyde and alcohol substrates such as here. Note that 3-unsubstituted indoles react with acyl halides by F-C acylation at the 3 position example
answered 1 hour ago
WaylanderWaylander
7,04811424
$endgroup$
add a comment |
$begingroup$
The heterocycle in this question is indole and is aromatic. This means that the N lone pair is delocalised and not readily available for nucleophilic attack. Think of it as similar in reactivity to a secondary amide nitrogen RCONHR. Generally you need to formally deprotonate to functionalise though there are some interesting techniques using carbonyl azoles catalysed by DBU reference and others using aldehyde and alcohol substrates such as here. Note that 3-unsubstituted indoles react with acyl halides by F-C acylation at the 3 position example
answered 1 hour ago
WaylanderWaylander
7,04811424
$endgroup$
The heterocycle in this question is indole and is aromatic. This means that the N lone pair is delocalised and not readily available for nucleophilic attack. Think of it as similar in reactivity to a secondary amide nitrogen RCONHR. Generally you need to formally deprotonate to functionalise though there are some interesting techniques using carbonyl azoles catalysed by DBU reference and others using aldehyde and alcohol substrates such as here. Note that 3-unsubstituted indoles react with acyl halides by F-C acylation at the 3 position example
answered 1 hour ago
WaylanderWaylander
7,04811424
answered 1 hour ago
WaylanderWaylander
7,04811424
answered 1 hour ago
WaylanderWaylander
7,04811424
answered 1 hour ago
WaylanderWaylander
7,04811424
7,04811424
add a comment |
add a comment |
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$begingroup$
Secondary amine group shown here is quite sterically hindered..Approach at Burgi-Dunitz trajectory would most probably be difficult
$endgroup$
– YUSUF HASAN
3 hours ago
$begingroup$
Did you mean lone pair of electron in N is less available for carbocation to be attacked? @YUSUFHASAN
$endgroup$
– Amar30657
3 hours ago
$begingroup$
No..I mean what you have in mind is a nucleophilic attack by NH on CH3COCl as the first step, right? So that would be retarded by steric hindrance..
$endgroup$
– YUSUF HASAN
3 hours ago
1
$begingroup$
Nothing to do with sterics. The lone pair on the nitrogen is delocalised into the aromatic system so is not available for nucleophilic attack. If you want to functionalise the indole-NH you generally have to formally deprotonate with strong base. Otherwise it reacts as an enamine through the 3-position.
$endgroup$
– Waylander
3 hours ago
1
$begingroup$
@Amar30657 You need to read more about aromatic systems. en.wikipedia.org/wiki/Indole
$endgroup$
– Waylander
3 hours ago