Hydrochloric Acid → HCID 117772329, compound
Reaction equation
[ClH:1].[OH:2][CH2:3][CH2:4][N:5]1[CH2:9][CH2:8][C@H:7]([NH:10]C(=O)OC(C)(C)C)[CH2:6]1>O1CCOCC1>[ClH:1].[NH2:10][C@H:7]1[CH2:8][CH2:9][N:5]([CH2:4][CH2:3][OH:2])[CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4M HCl solution (in dioxane) (1.5 mL) was added to a stirred solution of (S)-tert-butyl (1-(2-hydroxyethyl)pyrrolidin-3-yl)carbamate (400 mg, 1.73 mmol) in Dioxane (1 mL) and stirring was continued at 20-35° C. for 2 h. After which the reaction mixture was concentrated under reduced pressure to afford the crude. The crude obtained was purified by washing with diethyl ether and dried to afford 300 mg (crude) of the title compound.
Workup
- concentrationAfter which the reaction mixture was concentrated under reduced pressure
- customto afford the crude
- customThe crude obtained
- customwas purified
- washby washing with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-0ee7c32e99b540c59174a4e46824323c
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09289419B2
Reaction notes
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