Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,1,1,3,3,3-Hexafluoro-2-isocyanatopropane | HCID 12548132 | — |
| Reactant | HCID 69675374 | HCID 69675374 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86666512 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933085B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-910c294137ce4dfabe527065641d041c |
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| Source note | uspto-grants-2015_01 |
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