Hydrochloric Acid → 1029715-20-5
Reaction equation
C(OC(=O)[NH:7][CH:8]1[CH2:12][CH2:11][N:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[CH2:9]1)(C)(C)C.[ClH:20]>CO.O1CCOCC1>[ClH:20].[ClH:20].[N:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[N:10]1[CH2:11][CH2:12][CH:8]([NH2:7])[CH2:9]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
tert-Butyl(1-pyridin-2-ylpyrrolidin-3-yl)carbamate (2.5 g) was dissolved in methanol (4 mL) and was treated with 4M hydrogen chloride in 1,4-dioxane (8 mL). The mixture was stirred overnight at RT. The solvents were evaporated under reduced pressure. The residue was washed with ether and dried to give the desired product (2.1 g, 92%). LCMS: (M+H)=164.1.
Workup
- customThe solvents were evaporated under reduced pressure
- washThe residue was washed with ether
- customdried
Sources & evidence
- ORD record
- ord-766c3e3aded34bbb83271c2b63e1f3cd
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461330B2
Reaction notes
Loading…