Hydrochloric Acid → HCID 86762253, compound
Reaction equation
[F:1][C:2]1[S:6][C:5]([C@:7]23[CH2:15][N:14]([C:16]4[N:21]=[CH:20][CH:19]=[CH:18][N:17]=4)[CH2:13][C@H:12]2[CH2:11][S:10][C:9]([NH2:22])=[N:8]3)=[CH:4][CH:3]=1.[ClH:23]>C(OCC)C.ClCCl>[ClH:23].[F:1][C:2]1[S:6][C:5]([C@:7]23[CH2:15][N:14]([C:16]4[N:17]=[CH:18][CH:19]=[CH:20][N:21]=4)[CH2:13][C@H:12]2[CH2:11][S:10][C:9]([NH2:22])=[N:8]3)=[CH:4][CH:3]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred clear colorless solution of the [(4aR,7aR)-7a-(5-fluorothiophen-2-yl)-6-(pyrimidin-2-yl)-4,4a,5,6,7,7a-hexahydropyrrolo[3,4-d][1,3]thiazin-2-amine (318 mg, 948 μmol) in diethyl ether (10 mL) and dichloromethane (10 mL) is added a solution of 1 M HCl in diethyl ether (1.05 mL, 1.05 mmol). The resulting white mixture is stirred for a few minutes, then the solid is collected and washed with diethyl ether (15 mL), to give the title compound (325 mg, 92%) as a white solid. ES/MS (m/e): 336.0 (M+H).
Workup
- customthe solid is collected
- washwashed with diethyl ether (15 mL)
Sources & evidence
- ORD record
- ord-ff049e61700949c1a23ae8c3c1e55d28
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889856B2
Reaction notes
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