Hydrochloric Acid → HCID 45088410, compound
Reaction equation
[CH:1]1([N:4]([CH3:12])[C:5]([C@H:7]2[CH2:11][CH2:10][CH2:9][NH:8]2)=O)[CH2:3][CH2:2]1.B.Cl>C1COCC1>[CH:1]1([N:4]([CH3:12])[CH2:5][C@H:7]2[CH2:11][CH2:10][CH2:9][NH:8]2)[CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (R)-pyrrolidine-2-carboxylic acid cyclopropyl-methyl-amide (540 mg, 3.21 mmol) in THF (5 mL) at 0° C. was added borane (6.4 mL, 2 eq., 1 M in THF) dropwise. The mixture was allowed to warm up to rt then heated to reflux for 24 hours. The cooled reaction was acidified with HCl and heated at 75° C. for 10 mins. The mixture was concentrated, basified with 2N NaOH and extracted with 10% methanol in DCM. The combined DCM was dried and concentrated to give cyclopropyl-methyl-(R)-1-pyrrolidin-2-ylmethyl-amine.
Workup
- temperaturethen heated
- temperatureto reflux for 24 hours
- customThe cooled reaction
- temperatureheated at 75° C. for 10 mins
- concentrationThe mixture was concentrated
- extractionextracted with 10% methanol in DCM
- dry with materialThe combined DCM was dried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-7232069b332a4ecfbf9b4636b19e86fd
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06599902B2
Reaction notes
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