2,3-Dihydro-7-azaindole
CAS: 10592-27-5
Ref. 3D-FD74832
| 2g | To inquire | |
| 5g | To inquire | |
| 10g | To inquire | |
| 25g | To inquire | |
| 50g | To inquire |
Product Information
- 1H-Pyrrolo[2,3-b]pyridine, 2,3-dihydro-
- 7-Azaindoline
- 1H,2H,3H-pyrrolo[2,3-b]pyridine
2,3-Dihydro-7-azaindole is a hydrogen bond donor and a nucleophile. It has been shown to react with acetylcholine to produce the amide 2,3-dihydro-7-azaindolone. The reaction mechanism for this reaction is thought to involve protonation of the nitrogen atom in the amide group followed by nucleophilic attack on the carbonyl carbon of acetylcholine. This reaction is stereoselective because it can occur from either face of the chiral center on acetylcholine.
2,3-Dihydro-7-azaindole is synthesized by reacting an acid with an enolate ion derived from an α,β-unsaturated ketone or aldehyde. This synthesis produces a mixture of diastereomers that are separated by recrystallization or chromatography.
Chemical properties
Technical inquiry about: 3D-FD74832 2,3-Dihydro-7-azaindole
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