5,10-dihydro-4H-thieno[3,2-c][2]benzazepine → HCID 22099977, compound

HRID 1457677Notes

Reaction equation

HRID 1457677 reaction equation
[S:1]1[C:10]2[CH2:9][C:8]3[CH:11]=[CH:12][CH:13]=[CH:14][C:7]=3[CH2:6][NH:5][C:4]=2[CH:3]=[CH:2]1.[C:15]1([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:21]([NH:23][C:24]1[N:29]=[CH:28][C:27]([C:30](Cl)=[O:31])=[CH:26][CH:25]=1)=[O:22]>>[S:1]1[C:10]2[CH2:9][C:8]3[CH:11]=[CH:12][CH:13]=[CH:14][C:7]=3[CH2:6][N:5]([C:30]([C:27]3[CH:26]=[CH:25][C:24]([NH:23][C:21]([C:16]4[C:15]([C:33]5[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=5)=[CH:20][CH:19]=[CH:18][CH:17]=4)=[O:22])=[N:29][CH:28]=3)=[O:31])[C:4]=2[CH:3]=[CH:2]1

Participants

3

Procedure

As described for Example 12, 5,10-dihydro-4H-thieno[3,2-c][2]benzazepine is reacted with 6-[([1,1'-biphenyl]-2-ylcarbonyl)amino]-3-pyridinecarbonyl chloride to give the product as a solid.

Sources & evidence

ORD record
ord-773ca672b14d48fd876ac5b8b00b6df4
Source dataset
uspto-grants-1998_12
Patent number
US05849735

Reaction notes

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