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N-[4-(5-oxo-3,4-dihydro-2H-1-benzazepine-1-carbonyl)phenyl]-2-phenylbenzamide → HCID 129720332, compound

HRID 342305
Notes
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Reaction equation

HRID 342305 reaction equation
[C:1]1([C:7]2[CH:35]=[CH:34][CH:33]=[CH:32][C:8]=2[C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15](C(N3C4C=CC=CC=4C(=O)CCC3)=O)=[CH:14][CH:13]=2)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:36].N1C=CC=C(CC(N)=S)C=1>>[ClH:36].[C:1]1([C:7]2[CH:35]=[CH:34][CH:33]=[CH:32][C:8]=2[C:9]([NH:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[O:10])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 11798200N-[4-(5-oxo-3,4-dihydro-2H-1-benzazepine-1-carbonyl)phenyl]-2-phenylbenzamideHCID 867521833-Pyridylthioacetamide hydrochloride

Product 1

HCID 129720332HCID 129720332, compound

Procedure

Using 400 mg of 2-phenyl-4'-[(5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)carbonyl]benzanilide and 400 mg of 3-pyridylthioacetamide hydrochloride, the procedure of Example 5 was repeated to obtain 100 mg of 4'-[[2-(3-pyridylmethyl)-5,6-dihydro-4H-thiazolof5,4-d][1]benzazepin-6-yl)carbonyl]-2-phenylbenzanilide hydrochloride as an amorphous solid.

Sources & evidence

ORD record
ord-41774fc8e45647aaac6b70eb2ac11c78
Source dataset
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05856564

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes