Hydrochloric Acid → HCID 86677737, compound

HRID 1499813Notes

Reaction equation

HRID 1499813 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:35][CH2:36][CH3:37])=[C:18]([CH:24]4[CH2:27][N:26](C(OC(C)(C)C)=O)[CH2:25]4)[C:19]([F:23])=[C:20]([Cl:22])[CH:21]=3)[CH3:15])[N:9]=[C:10]([CH:11]([F:13])[F:12])[C:3]=12.[ClH:38].O1CCOCC1>ClCCl>[ClH:22].[ClH:38].[NH:26]1[CH2:27][CH:24]([C:18]2[C:17]([O:35][CH2:36][CH3:37])=[C:16]([CH:14]([N:8]3[C:4]4=[N:5][CH:6]=[N:7][C:2]([NH2:1])=[C:3]4[C:10]([CH:11]([F:13])[F:12])=[N:9]3)[CH3:15])[CH:21]=[C:20]([Cl:22])[C:19]=2[F:23])[CH2:25]1

Participants

5

Procedure

To a solution of tert-butyl 3-(3-{1-[4-amino-3-(difluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]ethyl}-5-chloro-2-ethoxy-6-fluorophenyl)azetidine-1-carboxylate (0.64 g, 1.2 mmol) in dichloromethane (5 mL) was added 4.0 M hydrogen chloride in dioxane (2.4 mL, 9.5 mmol). The reaction solution was stirred at room temperature for 6 h. The solvent was removed to give the desired product as a white solid (0.61 g, 100%). LCMS calculated for C19H21ClF3N6O (M+H)+: m/z=441.1; Found:441.1.

Workup

  1. customThe solvent was removed

Sources & evidence

ORD record
ord-c89e6f1099034cc6a7d1abb8fd7a71b5
Source dataset
uspto-grants-2015_12
Patent number
US09199982B2

Reaction notes

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