Hydrochloric Acid → HCID 66823991, compound
Reaction equation
[Si]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C@@H:15]2[C:20]3=[N:21][S:22](=[O:26])(=[O:25])[CH2:23][CH2:24][N:19]3[CH2:18][CH2:17][CH2:16]2)=[CH:11][CH:10]=1)(C(C)(C)C)(C)C.Cl>CO>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([C@@H:15]2[C:20]3=[N:21][S:22](=[O:26])(=[O:25])[CH2:23][CH2:24][N:19]3[CH2:18][CH2:17][CH2:16]2)=[CH:13][CH:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
A mixture of (9R)-9-(4-((tert-butyldimethylsilyl)oxy)phenyl)-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide (11.8 g) and 6 M HCl aq. (15.0 mL) in MeOH (100 mL) was stirred at 60° C. for 2 hr. After cooling to room temperature, the precipitate was collected and washed with MeOH to give the title compound (8.04 g) as a white solid.
Workup
- temperatureAfter cooling to room temperature
- customthe precipitate was collected
- washwashed with MeOH
Sources & evidence
- ORD record
- ord-37e2fc2baa1742dfad5f7e86c57f69e8
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150591B2
Reaction notes
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