Hydrochloric Acid → HCID 70207318, compound
Reaction equation
C(OC([NH:8][CH2:9][C@H:10]1[C@H:14]([C:15]([F:18])([F:17])[F:16])[CH2:13][NH:12][CH2:11]1)=O)(C)(C)C.FC(F)(F)C(O)=O.Cl>ClCCl>[NH2:8][CH2:9][C@H:10]1[C@H:14]([C:15]([F:18])([F:16])[F:17])[CH2:13][NH:12][CH2:11]1Participants
5
Conditions
- Temperature
- 0 °C
Procedure
In 1 ml of dichloromethane, is dissolved 202 mg (0.754 mmol) of trans-3-(tert-butoxycarbonylaminomethyl)-4-trifluoromethylpyrrolidine. To the above solution, is added 1 ml of trifluoroacetic acid on cooling with ice, and the mixture is stirred at 0° C. for 1 hour. To the reaction mixture, is added 0.19 ml of conc-hydrochloride, and the mixture was concentrated under reduced pressure to give 161 mg of the objective substance as a slightly yellow powder (yield 88.6%).
Workup
- temperatureon cooling with ice
- concentrationthe mixture was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-309054bc17104c7da262620b31d23a7b
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05668147
Reaction notes
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