(s)-Tert-butyl 5-methyl-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide → HCID 69415501, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([CH3:15])=[C:10]([C:16]([F:19])([F:18])[F:17])[CH:9]=2)=[O:5])[CH3:2].[C:20]([O:24][C:25]([N:27]1[CH2:31][C@H:30]([CH3:32])OS1(=O)=O)=[O:26])([CH3:23])([CH3:22])[CH3:21]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([C@H:30]([CH3:32])[CH2:31][NH:27][C:25]([O:24][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:26])[C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([CH3:15])=[C:10]([C:16]([F:19])([F:17])[F:18])[CH:9]=2)=[O:5])[CH3:2]Participants
3
Procedure
The title compound, m.p.: 103–105° C., EI-MS: m/e=428.1 (M+) and αD20=−40.3, was prepared in accordance with the general method of example 12b) from 5-methyl-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester and (S)-5-methyl-2,2-dioxo-[1,2,3]oxathiazolidine-3-carboxylic acid tert-butyl ester.
Sources & evidence
- ORD record
- ord-f9d8c09cf48747f9927291648db2aafd
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253281B2
Reaction notes
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