Aniline → HCID 117830894, compound

HRID 515908Notes

Reaction equation

HRID 515908 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[C:9]1[CH:10]=[C:11]2[CH:17]=[CH:16][N:15]([CH3:18])[C:12]2=[N:13][CH:14]=1>>[CH3:18][N:15]1[C:12]2=[N:13][C:14]([NH:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)=[CH:9][CH:10]=[C:11]2[CH:17]=[CH:16]1

Participants

3

Reactant 2

HCID 6115AnilineHCID 152962695-Bromo-1-methyl-1H-pyrrolo[2,3-b]pyridine

Product 1

HCID 117830894HCID 117830894, compound

Procedure

The procedure is in accordance with the protocol of Step B of Preparation 1″ using aniline and 5-bromo-1-methyl-1H-pyrrolo[2,3-b]pyridine (obtained in accordance with a protocol from the literature: Heterocycles, 60(4), 865, 2003).

Workup

  1. customThe procedure is in accordance with the protocol of Step B of Preparation 1″
  2. customobtained in accordance with a protocol from the literature

Sources & evidence

ORD record
ord-733752c77fcc43acae4155fef55b2ca9
Source dataset
uspto-grants-2015_08
Patent number
US09108983B2

Reaction notes

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