Hydrochloric Acid → HCID 73603937, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH2:4][C@@H:5]2[CH2:10][N:9]([C:11]3[N:16]=[C:15]([C:17]([OH:20])([CH3:19])[CH3:18])[C:14]([F:21])=[CH:13][N:12]=3)[CH2:8][C@:6]2([C:22]2[CH:27]=[N:26][CH:25]=[CH:24][N:23]=2)[N:7]=1.[ClH:28]>C(#N)C>[ClH:28].[NH2:1][C:2]1[S:3][CH2:4][C@@H:5]2[CH2:10][N:9]([C:11]3[N:16]=[C:15]([C:17]([OH:20])([CH3:18])[CH3:19])[C:14]([F:21])=[CH:13][N:12]=3)[CH2:8][C@:6]2([C:22]2[CH:27]=[N:26][CH:25]=[CH:24][N:23]=2)[N:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[2-[(4aR,7aR)-2-amino-7a-pyrazin-2-yl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-6-yl]-5-fluoro-pyrimidin-4-yl]propan-2-ol (120 mg, 0.308 mmol) is dissolved in 0.1 M HCl (3.1 mL) and acetonitrile (1 mL). The resulting solution is freeze dried to obtain the title compound as a white solid. ES/MS (m/e): 390 (M+1).
Workup
- customdried
Sources & evidence
- ORD record
- ord-1b851fd48198424db33a3927a15df3fb
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09328124B2
Reaction notes
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