Sodium ethanethiolate → HCID 11397140, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][CH2:16]O)[CH2:10][CH:9]1[C:18](=[O:35])[NH:19][CH:20]([CH:24]1[CH:29]([OH:30])[CH:28]([OH:31])[CH:27]([OH:32])[CH:26]([S:33][CH3:34])[O:25]1)[CH:21]([CH3:23])[CH3:22])=O)(C)(C)C.[CH2:36]([S-:38])[CH3:37].[Na+]>>[CH3:22][CH:21]([CH3:23])[CH:20]([NH:19][C:18]([CH:9]1[CH2:10][CH:11]([CH2:14][CH2:15][CH2:16][S:38][CH2:36][CH3:37])[CH2:12][CH2:13][NH:8]1)=[O:35])[CH:24]1[CH:29]([OH:30])[CH:28]([OH:31])[CH:27]([OH:32])[CH:26]([S:33][CH3:34])[O:25]1Participants
3
Procedure
The title compound of example 22 was prepared from protected tosylate intermediate prepared in example 19, according to the procedure used in examples 19–21, using sodium ethanethiolate in the displacement step; MS (ESPOS): 465.3 [M+H]+.
Sources & evidence
- ORD record
- ord-4994f61edfc34fdfaa3be4b2c85488e4
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07199106B2
Reaction notes
Loading…