Hydrochloric Acid → HCID 90203546, compound
Reaction equation
C(OC([N:8]1[CH2:12][C:11]([CH3:14])([CH3:13])[CH2:10][CH:9]1[C:15](=[O:17])[NH2:16])=O)(C)(C)C.[ClH:18].C(OCC)C>O1CCOCC1>[ClH:18].[CH3:13][C:11]1([CH3:14])[CH2:12][NH:8][CH:9]([C:15]([NH2:16])=[O:17])[CH2:10]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-carbamoyl-4,4-dimethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.2 g, 4.95 mmol) in dioxane (5 mL) was cooled to 10° C. Hydrogen chloride dissolved in dioxane (10 mL, 6.4 N) was added and the mixture was stirred for 1.5 hours. Diethylether (50 mL) was added to completely precipitate the product, which was filtered and dried to give the title compound (0.84 g, 95%) as colorless solid; MS (ESI) 143.0 [MH+].
Workup
- additionwas added
- customto completely precipitate the product, which
- filtrationwas filtered
- customdried
Sources & evidence
- ORD record
- ord-61a01339f9994437a27bdf85444d7f59
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09303012B2
Reaction notes
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