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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260728Generated: October 31, 2026

Triethylamine → HCID 178505143, compound

https://huagongshe.com/reaction/1260728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178478590HCID 178478590—
SolventDichloromethaneHCID 6344—
ProductHCID 178505143HCID 17850514366%

Reaction Steps

To a stirred mixture of trans-4-{2-[4-(2,3-dihydro-furo[2,3-c]pyridin-7-yl)-piperazin-1-yl]-ethyl}-cyclohexylamine trihydrochloride (intermediate B) (70.4 mg, 0.16 mmol) in dichloromethane (1 ml) was added at room temperature triethylamine (89 mg, 123 μl, 880 μmol) and methanesulfonyl chloride (27.5 mg, 18.7 μl, 240 μmol). The mixture was allowed to stir at room temperature for 18 h, poured into ice/water (5 ml) and 1N sodium hydroxide solution (5 ml) and extracted with dichloromethane (2×15 ml). The combined organic layers were washed with brine (15 ml), dried (MgSO4) and evaporated. The crude material was further purified by flash chromatography on silica gel (dichloromethane/MeOH 9:1) and trituration with dichloromethane (1 ml) and heptane (5 mL) for 30 min to yield the title compound as an off-white solid (43 mg, 66%), MS (ISP) m/z=409.4 [(M+H)+], mp 220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470828B2
Source datasetuspto-grants-2013_06
ORD IDord-01424643e4ce4769bc28ab938e830b62
Source noteuspto-grants-2013_06