4-Benzoylbenzoyl chloride → HCID 22099540, compound

HRID 1457688Notes

Reaction equation

HRID 1457688 reaction equation
[S:1]1[C:5]2[CH2:6][NH:7][C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[CH2:10][C:4]=2[CH:3]=[CH:2]1.[C:15]([C:23]1[CH:31]=[CH:30][C:26]([C:27](Cl)=[O:28])=[CH:25][CH:24]=1)(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[C:15]([C:23]1[CH:24]=[CH:25][C:26]([C:27]([N:7]2[C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[CH2:10][C:4]3[CH:3]=[CH:2][S:1][C:5]=3[CH2:6]2)=[O:28])=[CH:30][CH:31]=1)(=[O:22])[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 129121414-Benzoylbenzoyl chlorideHCID 15288194HCID 15288194, compound

Product 1

HCID 22099540HCID 22099540, compound

Procedure

As described for Example 26, 9,10-dihydro-4H-thieno[2,3-c][1]benzazepine is reacted with 4-(benzoyl)benzoyl chloride to give the product as a solid.

Sources & evidence

ORD record
ord-2668df81ac3e4beba963ece80b096cd4
Source dataset
uspto-grants-1998_12
Patent number
US05849735

Reaction notes

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