HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289299Generated: October 30, 2026
Methanesulfonyl chloride → HCID 15840421, compound
https://huagongshe.com/reaction/2289299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18700152 | HCID 18700152 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15840421 | HCID 15840421 | — |
Reaction Steps
To a solution of 1-(1-(4-(4-piperidinyloxy)-2-(2,2,2-trifluoroethoxy)phenylacetyl)piperidin-4-yl)-4H-3,1-benzoxazin-2(1H)-one hydrochloride (0.20 g, 0.35 mmol) from Example 2 in CH2Cl2 (20 mL) was added methanesulfonoyl chloride (0.045 g, 0.39 mmol) and DIEA (0.14 mL, 0.80 mmol). The solution was stirred at ambient temperature for 6 h and the solvent was removed under reduced pressure. The residue was dissolved in EtOAc (50 mL) and washed with 0.25 M aqueous citric acid (25 mL), H2O (25 mL), and saturated aqueous NaHCO3 (25 mL). The organic phase was dried (MgSO4), filtered, and the solvent was removed under reduced pressure. The residue was purified by pressurized silica gel column chromatography using 97:3 CH2Cl2 :MeOH as eluant to give the title compound as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090805 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-649b6a4f21f04380b04f9abcae54dfc6 |
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| Source note | uspto-grants-2000_07 |
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