2-Chloro-3-pyridylamine → [2-[(3-Amino-2-pyridinyl)amino]phenyl](4-pyridinyl)methanone

HRID 979603

Reaction equation

HRID 979603 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:10]1[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=1)=[O:9].[NH2:16][C:17]1[C:18](Cl)=[N:19][CH:20]=[CH:21][CH:22]=1>>[NH2:16][C:17]1[C:18]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[C:8]([C:10]2[CH:11]=[CH:12][N:13]=[CH:14][CH:15]=2)=[O:9])=[N:19][CH:20]=[CH:21][CH:22]=1

Participants

3

Procedure

The title compound is prepared by reacting (2-aminophenyl)(4-pyridinyl)methanone as prepared by Nann, A. J. and Schofield, K., J. Chem. Soc. 1952, 583-9 with 3-amino-2-chloropyridine.

Workup

  1. customas prepared by Nann

Sources & evidence

ORD record
ord-77667d1b3a3e4396a86b3e9f76cc0f1d
Source dataset
uspto-grants-1987_05
Patent number
US04668675

Linked notes

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