HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914526Generated: November 1, 2026
Methanesulfonyl chloride → HCID 66832667, compound
https://huagongshe.com/reaction/1914526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66832471 | HCID 66832471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66832667 | HCID 66832667 | — |
Reaction Steps
To a solution of [2-(4-trifluoromethyl-phenyl)-pyrimidin-4-yl]-methanol (110 mg, 0.43 mmol), diisopropylethylamine (0.10 mL, 0.52 mmol), and CH2Cl2 (5 mL) was added methanesulfonyl chloride (37 μL, 0.47 mmol). After 1 h, the resulting solution was concentrated. The residue was re-dissolved in 7N NH3 in MeOH (10 mL) and heated to 70° C. in a sealed tube. After 1 h, the resulting solution was cooled, concentrated, and the residue was used crude (110 mg, 100%). MS (ESI): mass calcd. for C12H10F3N3, 253.0; m/z found, 254.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614201B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-6cc531a7a7c84fb796a963bed292f5dc |
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| Source note | uspto-grants-2013_12 |
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