Hydrochloric Acid → HCID 19090437, compound
Reaction equation
[ClH:1].C(OC([NH:9][CH2:10][CH2:11][C:12]1[S:13][C:14]2[NH:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]=2[N:21]=1)=O)(C)(C)C>CO>[ClH:1].[ClH:1].[NH2:9][CH2:10][CH2:11][C:12]1[S:13][C:14]2[NH:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]=2[N:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution (3 ml) of 4.75N hydrochloric acid in methanol was added to a solution (10 ml) of 2-[2-(tert-butoxycarbonyl- amino)ethyl]-5,6,7,8-tetrahydro-4H-thiazolo -[5,4-b]azepine (1.00 g) in methanol, and the whole was stirred for 5 hrs. at room temperature. The solvent was distilled off under reduced pressure. The residue was washed with ethyl ether, and recrystallized from a mixture of methanol and ethyl ether to give the title compound (0.64 g, 70.5%).
Workup
- customat room temperature
- distillationThe solvent was distilled off under reduced pressure
- washThe residue was washed with ethyl ether
- customrecrystallized from a mixture of methanol and ethyl ether
Sources & evidence
- ORD record
- ord-dfa5490612244b68bf81c44c2f941187
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300639
Reaction notes
Loading…