4-Fluorobenzoyl chloride → 5-(N-[4-fluorobenzoyl]amino)-3-(1-(2-phenyleth-1yl)-1,2,3,6-tetrahydropyridin-4yl)pyrrolo[3,2-b]pyridine

HRID 581348Notes

Reaction equation

HRID 581348 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]2[C:8]([C:11]3[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH2:15][CH:16]=3)=[CH:9][NH:10][C:5]2=[CH:4][CH:3]=1.[F:25][C:26]1[CH:34]=[CH:33][C:29]([C:30](Cl)=[O:31])=[CH:28][CH:27]=1>>[F:25][C:26]1[CH:34]=[CH:33][C:29]([C:30]([NH:1][C:2]2[N:7]=[C:6]3[C:8]([C:11]4[CH2:12][CH2:13][N:14]([CH2:17][CH2:18][C:19]5[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=5)[CH2:15][CH:16]=4)=[CH:9][NH:10][C:5]3=[CH:4][CH:3]=2)=[O:31])=[CH:28][CH:27]=1

Participants

3

Reactant 2

HCID 678794-Fluorobenzoyl chlorideHCID 110992005-Amino-3-(1-(2-phenyleth-1-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyrrolo[3,2-b]pyridine

Product 1

HCID 196016115-(N-[4-fluorobenzoyl]amino)-3-(1-(2-phenyleth-1yl)-1,2,3,6-tetrahydropyridin-4yl)pyrrolo[3,2-b]pyridine

Procedure

Beginning with 0.015 gm (0.047 mMol) 5-amino-3-(1-(2-phenyleth-1-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyrrolo[3,2-b]pyridine and 0.007 mL (0.061 mMol) 4-fluorobenzoyl chloride, the title compound was prepared essentially by the procedure described in Example 7.

Sources & evidence

ORD record
ord-ad8eed716d4a418e8ef509ef4f1d6bc5
Source dataset
uspto-grants-1999_07
Patent number
US05919936

Reaction notes

Loading…