2-Chloro-3-pyridylamine → HCID 20200298, compound

HRID 543610Notes

Reaction equation

HRID 543610 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=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]=[N:12][CH:13]=[CH:14][CH:15]=2)=[O:9])=[N:19][CH:20]=[CH:21][CH:22]=1

Participants

3

Reactant 2

HCID 805282-Chloro-3-pyridylamineHCID 21842372HCID 21842372, compound

Product 1

HCID 20200298HCID 20200298, compound

Procedure

The title compound is prepared by reacting (2-aminophenyl)(3-pyridinyl)methanone as prepared by Abramovitch R. A. & Tertzakian, G., Tetrahedron Letters, 1963, 1511-15 and Abramovitch, R. A. et al., Can. J. Chem. 43(4), 725-31 (1965) with 3-amino-2-chloropyridine.

Workup

  1. customas prepared by Abramovitch R

Sources & evidence

ORD record
ord-140374c891904169b0109084e3a42ab6
Source dataset
uspto-grants-1984_05
Patent number
US04447361

Reaction notes

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