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Aniline → HCID 13936025, compound

HRID 2292035
Notes
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Reaction equation

HRID 2292035 reaction equation
ClC1C=C(C=CC=1)C(O[CH:8]1[C:13](=[O:14])[NH:12][C:11]([CH3:15])=[C:10]([C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)[S:9]1)=O.[NH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[CH3:15][C:11]1[NH:12][C:13](=[O:14])[CH:8]([NH:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[S:9][C:10]=1[C:16]1[CH:17]=[CH:18][N:19]=[CH:20][CH:21]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6115AnilineHCID 139360302-(3-chlorobenzoyloxy)-5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one

Product 1

HCID 13936025HCID 13936025, compound

Procedure

2-(3-Chlorobenzoyloxy)-5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one and aniline were reacted to give the titled compound as pale yellow crystals.

Sources & evidence

ORD record
ord-67b577db636b40aba53d1f70ac0861e6
Source dataset
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04800201

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes