4-[([1,1'-Biphenyl]-2-carbonyl)amino]-2-chlorobenzoyl chloride → HCID 22099678, compound

HRID 1457704Notes

Reaction equation

HRID 1457704 reaction equation
[CH:1]1[S:2][CH:3]=[C:4]2[C:10]=1[CH2:9][NH:8][C:7]1[CH:11]=[CH:12][CH:13]=[CH:14][C:6]=1[NH:5]2.[C:15]1([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[C:16]([C:21]([NH:23][C:24]2[CH:32]=[CH:31][C:27](C(Cl)=O)=[C:26]([Cl:33])[CH:25]=2)=[O:22])=[CH:17][CH:18]=[CH:19][CH:20]=1>>[CH:1]1[S:2][CH:3]=[C:4]2[C:10]=1[CH2:9][N:8]([C:27]1[CH:31]=[CH:32][C:24]([NH:23][C:21]([C:16]3[C:15]([C:34]4[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=4)=[CH:20][CH:19]=[CH:18][CH:17]=3)=[O:22])=[CH:25][C:26]=1[Cl:33])[C:7]1[CH:11]=[CH:12][CH:13]=[CH:14][C:6]=1[NH:5]2

Participants

3

Procedure

As described for Example 400, 9,10-dihydro-4H-thieno[3,4-b][1,5]benzodiazepine is reacted with 4-[([1,1'-biphenyl]-2-carbonyl)amino]-2-chlorobenzoyl chloride to give the product as a solid.

Sources & evidence

ORD record
ord-91249b1877b24098a6c8bc37c1d0f995
Source dataset
uspto-grants-1998_12
Patent number
US05849735

Reaction notes

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