HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472106Generated: October 30, 2026
Bromotrimethylsilane → HCID 178482412, compound
https://huagongshe.com/reaction/472106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22262455 | HCID 22262455 | — |
| Reactant | HCID 178482410 | HCID 178482410 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178482412 | HCID 178482412 | — |
Reaction Steps
(3R)-1-[({trans-4-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclohexyl}-methyl)sulfonyl]piperidin-3-ol (100 mg, 0.24 mmol) was suspended in dichloromethane (5 mL). Diisopropylethylamine (0.05 mL, 0.3 mmol) was added followed by diethyl chloro phosphate (0.036 mL, 0.24 mmol). The reaction mixture was stirred under nitrogen overnight. Methanol (1 mL) was added to the flask and the reaction mixture was concentrated in vacuo. The residue was dissolved in dichloromethane (10 mL) and bromotrimethylsilane (2 mL, 14.4 mmol) was added. The reaction mixture was stirred under nitrogen at room temperature for 18 hours and then was concentrated in vacuo. The residue was purified by reverse phase HPLC. (2 mg, 5%). 1H NMR (400 MHz, DMSO-d6) ppm 1.28 (br. s., 1H) 1.50 (br. s., 1H) 1.63-1.72 (m, 2H) 1.86 (d, J=2.56 Hz, 1H) 2.02 (d, J=10.98 Hz, 1H) 2.83 (s, 1H) 2.94 (td, J=14.46, 6.59 Hz, 2H) 3.14 (s, 2H) 3.47 (br. s., 9H) 3.52 (br. s., 11H) 6.51 (br. s., 1H) 7.09 (d, J=2.93 Hz, 1H). LCMS m/z 488.8 (M+H calcd for C19H30N6O6PS requires 487.5). LCMS (C-18 column, gradient elution 5 minute chromatograph, 95:5 to 5:95 water/acetonitrile, retention time 1.23 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633206B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-ff825593e7a643599de125c537334120 |
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| Source note | uspto-grants-2014_01 |
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