Hydrochloric Acid → HCID 86677719, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]2[N:8]([CH:14]([C:16]3[C:17]([O:36][CH3:37])=[C:18]([CH:25]4[CH2:28][N:27](C(OC(C)(C)C)=O)[CH2:26]4)[C:19]([CH3:24])=[C:20]([C:22]#[N:23])[CH:21]=3)[CH3:15])[N:9]=[C:10]([CH:11]([F:13])[F:12])[C:3]=12.[ClH:38].O1CCOCC1>C(Cl)Cl>[ClH:38].[ClH:38].[NH2:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]2[N:8]([CH:14]([C:16]3[C:17]([O:36][CH3:37])=[C:18]([CH:25]4[CH2:28][NH:27][CH2:26]4)[C:19]([CH3:24])=[C:20]([CH:21]=3)[C:22]#[N:23])[CH3:15])[N:9]=[C:10]([CH:11]([F:12])[F:13])[C:3]=12Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl 3-(3-{1-[4-amino-3-(difluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-5-cyano-2-methoxy-6-methylphenyl)azetidine-1-carboxylate (0.20 g, 0.39 mmol) in methylene chloride (5 mL) was added 4.0 M hydrogen chloride in 1,4-dioxane (0.60 mL, 2.4 mmol). The resulting mixture was stirred at room temp for 3.5 h. The solvents were evaporated and the residue dried in vacuo to give 0.23 g of the product as the HCl salt. LCMS calculated for C20H22F2N7O (M+H)+: m/z=414.2; Found: 414.1.
Workup
- customThe solvents were evaporated
- customthe residue dried in vacuo
Sources & evidence
- ORD record
- ord-fc3e55027f864c29b4f846fb1fc4fd05
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199982B2
Reaction notes
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