Formaldehyde → 1-(2-tert-Butyl-phenyl)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic Acid Ethyl Ester
Reaction equation
[CH2:1]([O:3][C:4](=[O:17])[CH2:5][NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]([CH3:16])([CH3:15])[CH3:14])[CH3:2].[CH2:18]=O.[CH:20]([S:22]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[C:31]([F:34])([F:33])[F:32])(=[O:24])=[O:23])=[CH2:21]>>[CH2:1]([O:3][C:4]([CH:5]1[CH2:18][CH:20]([S:22]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[C:31]([F:32])([F:34])[F:33])(=[O:23])=[O:24])[CH2:21][N:6]1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]([CH3:16])([CH3:15])[CH3:14])=[O:17])[CH3:2]Participants
4
Procedure
In analogy to the procedure described in example 343d, (2-tert-butyl-phenylamino)-acetic acid ethyl ester (CAS Reg. No. 959563-17-8) was reacted with paraformaldehyde and 1-ethenesulfonyl-2-trifluoromethyl-benzene (example 243c) to give the title compound as colorless oil. MS (ESI): m/z=484.4 [M+H]+.
Sources & evidence
- ORD record
- ord-b98f462caafd4813ba09f099a943a16a
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163793B2
Reaction notes
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