Benzoyl chloride → HCID 19818455, compound

HRID 1086812Notes

Reaction equation

HRID 1086812 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([C:15]1[S:16][C:17]([CH:21]([C:23]3[CH:28]=[CH:27][C:26]([CH2:29][CH:30]([CH3:32])[CH3:31])=[CH:25][CH:24]=3)[CH3:22])=[C:18](O)[N:19]=1)[CH3:14])[CH:7]=[CH:6]2.[C:33](Cl)(=[O:40])[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([C:15]1[S:16][C:17]([CH:21]([C:23]3[CH:28]=[CH:27][C:26]([CH2:29][CH:30]([CH3:32])[CH3:31])=[CH:25][CH:24]=3)[CH3:22])=[C:18]([C:33](=[O:40])[C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[N:19]=1)[CH3:14])[CH:7]=[CH:6]2

Participants

4

Procedure

The desired compound is prepared by treatment of the product of example 45 with benzoyl chloride and pyridine.

Sources & evidence

ORD record
ord-38e70ccc28694be1841dcf1061d7a57e
Source dataset
uspto-grants-1991_07
Patent number
US05032588

Reaction notes

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