Trifluoroacetic acid → (2R,4R)-4-hydroxy-pyrrolidine-2-carboxylic acid cyclopropylamide
Reaction equation
C(OC([N:8]1[CH2:12][C@H:11]([OH:13])[CH2:10][C@@H:9]1[C:14](=[O:19])[NH:15][CH:16]1[CH2:18][CH2:17]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH:16]1([NH:15][C:14]([C@H:9]2[CH2:10][C@@H:11]([OH:13])[CH2:12][NH:8]2)=[O:19])[CH2:18][CH2:17]1Participants
4
Procedure
(2R,4R)-2-Cyclopropylcarbamoyl-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester (5 g) was deprotected using 50 mL of 30% TFA in DCM at rt for 2 hours to give 3 g of (2R,4R)-4-hydroxy-pyrrolidine-2-carboxylic acid cyclopropylamide as a light yellow oil.
Workup
- customat rt
- customfor 2 hours
Sources & evidence
- ORD record
- ord-4716e4eee94b41a582fafb121492f75e
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06861418B2
Reaction notes
Loading…