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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772778Generated: November 3, 2026

Methanesulfonyl chloride → HCID 86651906, compound

https://huagongshe.com/reaction/1772778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67054912HCID 67054912—
SolventDichloromethaneHCID 6344—
ProductHCID 86651906HCID 86651906102.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of benzyl 4-(2-hydroxypropyl)piperazine-1-carboxylate (from step 1, 1.7 g, 6.1 mmol) in DCM (20 mL) was added DIPEA (2.1 mL, 12 mmol) followed by methanesulfonyl chloride (0.70 mL, 9.0 mmol) at 0° C. The reaction was stirred at 0° C. for 2 h. The reaction was quenched with saturated NaHCO3 solution and extracted with DCM. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to provide crude product (2.22 g) which was used in next step without further purification. LCMS calculated for C16H25N2O5S(M+H)+: m/z=357.1; Found: 357.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249145B2
Source datasetuspto-grants-2016_02
ORD IDord-ae22d9873b964d94b8a1f980554dabc4
Source noteuspto-grants-2016_02