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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426363Generated: November 4, 2026

Dichloromethane → HCID 86666512, compound

https://huagongshe.com/reaction/1426363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantM-XyleneHCID 7929—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1,1,3,3,3-Hexafluoro-2-isocyanatopropaneHCID 12548132—
ReactantHCID 69675374HCID 69675374—
SolventEthyl AcetateHCID 8857—
ProductHCID 86666512HCID 86666512—

Reaction Steps

To a solution of {3-piperazin-1-yl-1-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]cyclobutyl}acetonitrile (0.10 g, 0.20 mmol) in methylene chloride (5 mL, 80 mmol) was added. 0.21M 1,1,1,3,3,3-hexafluoro-2-isocyanatopropane in m-xylene (1.2 mL, 0.24 mmol) was added, followed by N,N-diisopropylethylamine (71 μL, 0.41 mmol). The reaction was stirred overnight. The reaction was rotovaped and ethyl acetate was added, washed with sat. NH4Cl (×2), sat. NaHCO3, and sat. NaCl. The extracts were dried and the solvent removed by rotary evaporation to give 164 mg of an orange oil. The crude oil was purified by column chromatography on 40 g silica gel using a gradient of 0-8% MeOH/DCM, 0-0.8% NH4Cl. The product was collected as 82 mg of a glass (59% yield). LCMS (M+1): 586.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-910c294137ce4dfabe527065641d041c
Source noteuspto-grants-2015_01