Hydrochloric Acid → HCID 86762254, compound
Reaction equation
[F:1][C:2]1[CH:3]=[N:4][C:5]([N:8]2[CH2:16][C@@H:15]3[C@@:10]([C:18]4[S:19][C:20]([F:23])=[CH:21][CH:22]=4)([N:11]=[C:12]([NH2:17])[S:13][CH2:14]3)[CH2:9]2)=[N:6][CH:7]=1.[ClH:24]>C(OCC)C>[ClH:24].[F:1][C:2]1[CH:7]=[N:6][C:5]([N:8]2[CH2:16][C@@H:15]3[C@@:10]([C:18]4[S:19][C:20]([F:23])=[CH:21][CH:22]=4)([N:11]=[C:12]([NH2:17])[S:13][CH2:14]3)[CH2:9]2)=[N:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred clear colorless solution of [(4aR,7aR)-6-(5-fluoropyrimidin-2-yl)-7a-(5-fluorothiophen-2-yl)-4,4a,5,6,7,7a-hexahydropyrrolo[3,4-d][1,3]thiazin-2-amine (255 mg, 722 μmol) and diethyl ether (10 mL) is added a solution of 1 M HCl in diethyl ether (794 μL, 794 μmol). The resulting white mixture is stirred for a few minutes and the resulting solid collected and rinsed with diethyl ether (10 mL), to give the title compound (274 mg, 97%) as a white solid. ES/MS (m/e): 354.0 (M+H).
Workup
- customthe resulting solid collected
- washrinsed with diethyl ether (10 mL)
Sources & evidence
- ORD record
- ord-4ecb166e6a804915b54afa7e0c66699c
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889856B2
Reaction notes
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