3-(Acetylthio)-2-methylpropanoic acid → HCID 13069272, compound
Reaction equation
C([S:4][CH2:5][CH:6]([CH3:10])[C:7]([OH:9])=O)(=O)C.[C:11]([CH:16]1[CH2:24][CH:23]2[CH:18]([CH2:19][CH2:20][CH2:21][CH2:22]2)[NH:17]1)([O:13]CC)=[O:12].C(C1CC2C(=CC=CC=2)N1)(OCC)=O>>[SH:4][CH2:5][CH:6]([CH3:10])[C:7]([N:17]1[CH:18]2[CH:23]([CH2:22][CH2:21][CH2:20][CH2:19]2)[CH2:24][CH:16]1[C:11]([OH:13])=[O:12])=[O:9]Participants
4
Procedure
Using the method described in example 1, beginning with 3-acetylthio 2-(RS) methylpropionic acid and 2-(RS) carbethoxy perhydroindole, prepared by reduction of 2(RS) carbethoxy indoline according to the method described in example 13, the following are obtained successively:
Workup
- customthe following are obtained successively
Sources & evidence
- ORD record
- ord-7c2843dcfefc450288da42f1e91fc300
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04404206
Reaction notes
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