Acetyl chloride → HCID 69507814, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:32])[C:5]1[C:10]([NH2:11])=[CH:9][CH:8]=[C:7]([C:12]2[CH2:16][CH2:15][CH2:14][C:13]=2[C:17]2[CH:22]=[C:21]([CH3:23])[CH:20]=[CH:19][C:18]=2[O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:6]=1)[CH3:2].[C:33](Cl)(=[O:35])[CH3:34]>>[CH2:1]([O:3][C:4](=[O:32])[C:5]1[C:10]([NH:11][C:33](=[O:35])[CH3:34])=[CH:9][CH:8]=[C:7]([C:12]2[CH2:16][CH2:15][CH2:14][C:13]=2[C:17]2[CH:22]=[C:21]([CH3:23])[CH:20]=[CH:19][C:18]=2[O:24][CH2:25][C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:6]=1)[CH3:2]Participants
3
Procedure
Prepared by general procedure E but using 3-{2-[5-methyl-2-(benzyloxy)phenyl]cyclopent-1-enyl}-6-aminobenzoic acid ethyl ester and acetyl chloride.
Workup
- customPrepared by general procedure E
Sources & evidence
- ORD record
- ord-1fd205902c3247b7a8e442cefcd4c1a3
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07232821B2
Reaction notes
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