Hydrochloric Acid → HCID 90232292, compound
Reaction equation
[F:1][C:2]([F:18])([F:17])[CH:3]1[CH2:8][CH:7]([NH:9]C(=O)OC(C)(C)C)[CH2:6][CH2:5][NH:4]1.[ClH:19]>C(OCC)C>[ClH:19].[F:18][C:2]([F:1])([F:17])[CH:3]1[CH2:8][CH:7]([NH2:9])[CH2:6][CH2:5][NH:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
115 mg (0.43 mmol) of tert-butyl [2-(trifluoromethyl)piperidin-4-yl]carbamate were initially charged in 2.2 ml of diethyl ether, 2.14 ml (4.28 mmol) of 2 N hydrochloric acid in diethyl ether were added and the mixture was stirred at RT overnight. The reaction mixture was concentrated and the residue was dried under high vacuum. 89 mg of the target compound were obtained (101% of theory).
Workup
- concentrationThe reaction mixture was concentrated
- customthe residue was dried under high vacuum
Sources & evidence
- ORD record
- ord-38be0c1ca2034475afbab1f972ef7096
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422285B2
Reaction notes
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