1-Bromoethyl acetate → HCID 88207518, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:31]/[OH:32])/[C:8]([NH:10][CH:11]2[C:29](=[O:30])[N:13]3[C:14]([C:26]([O-:28])=[O:27])=[C:15]([CH2:18][O:19][C:20]([N:22]4[CH2:25][CH2:24][CH2:23]4)=[O:21])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1.[Na+].[C:34]([O:37][CH:38](Br)[CH3:39])(=[O:36])[CH3:35]>>[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:31]/[OH:32])/[C:8]([NH:10][CH:11]2[C:29](=[O:30])[N:13]3[C:14]([C:26]([O:28][CH:38]([O:37][C:34](=[O:36])[CH3:35])[CH3:39])=[O:27])=[C:15]([CH2:18][O:19][C:20]([N:22]4[CH2:25][CH2:24][CH2:23]4)=[O:21])[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1Participants
3
Procedure
The compound obtained in Example 8 and 1-bromoethyl acetate were reacted, whereby the title compound was obtained.
Sources & evidence
- ORD record
- ord-0da5bf3521c54051923a05d6fb82e2f0
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05559225
Reaction notes
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