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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501474Generated: November 1, 2026

Methanesulfonyl chloride → HCID 178504221, compound

https://huagongshe.com/reaction/1501474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178504220HCID 178504220—
SolventChloroformHCID 6212—
ProductHCID 178504221HCID 178504221—

Reaction Conditions

Temperature0 °C

Reaction Steps

cis-4-[4-(7-[2-(Trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]cyclohexylmethanol was dissolved in chloroform (3.00 mL) and was cooled to 0° C. To the reaction was added TEA (0.10 mL, 0.00072 mol) and methanesulfonyl chloride (0.05 mL, 0.0006 mol) and this mixture was stirred at 0° C. for 2 hours at which time LCMS analysis showed mainly the product present in the mixture. The reaction was extracted with ethyl acetate and the organic extracts were washed with water, saturated NaCl, dried (MgSO4) and concentrated in vacuo. LC/MS (M+H)+: 506

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206187B2
Source datasetuspto-grants-2015_12
ORD IDord-8cc6bf6d359844b6aa316b4c163f4621
Source noteuspto-grants-2015_12