2-Chloro-3-pyridylamine → HCID 20200338, compound

HRID 543607Notes

Reaction equation

HRID 543607 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:10]1[S:11][CH:12]=[CH:13][CH:14]=1)=[O:9].[NH2:15][C:16]1[C:17](Cl)=[N:18][CH:19]=[CH:20][CH:21]=1>>[NH2:15][C:16]1[C:17]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[C:8]([C:10]2[S:11][CH:12]=[CH:13][CH:14]=2)=[O:9])=[N:18][CH:19]=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 805282-Chloro-3-pyridylamineHCID 12750529HCID 12750529, compound

Product 1

HCID 20200338HCID 20200338, compound

Procedure

In accordance with the procedure of Intermediate 9, (2-aminophenyl)(2-thienyl)methanone, prepared by the method of Steinkopf & Gunther, Ann. 522, 28-34 (1936), is reacted with 3-amino-2-chloropyridine to give the title compound.

Sources & evidence

ORD record
ord-f1137662a38844fa8bc0d93650158f8f
Source dataset
uspto-grants-1984_05
Patent number
US04447361

Reaction notes

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