Ethyl Glycolate → HCID 86586233, compound
Reaction equation
[F:1][C:2]1[CH:36]=[C:35]([F:37])[CH:34]=[CH:33][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:32]=[CH:31][C:20]([O:21][C:22]2[CH:23]=[C:24]([OH:30])[CH:25]=[C:26]([O:28][CH3:29])[CH:27]=2)=[CH:19][CH:18]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15].[C:38]([O:42][CH2:43][CH3:44])(=[O:41])[CH2:39]O>>[F:1][C:2]1[CH:36]=[C:35]([F:37])[CH:34]=[CH:33][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:32]=[CH:31][C:20]([O:21][C:22]2[CH:23]=[C:24]([CH:25]=[C:26]([O:28][CH3:29])[CH:27]=2)[O:30][CH2:39][C:38]([O:42][CH2:43][CH3:44])=[O:41])=[CH:19][CH:18]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15]Participants
3
Procedure
The product from Example 90E and ethyl glycolate were processed as described in Example 62A to provide the title compound. MS (ESI+) m/z 593 (M+H)+.
Sources & evidence
- ORD record
- ord-583df146c8f641db98240f63b1058170
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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