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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119490Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86591982, compound

https://huagongshe.com/reaction/2119490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 54107592HCID 54107592—
SolventPyridineHCID 1049—
ProductHCID 86591982HCID 8659198213%

Reaction Steps

To a solution containing 2-(4-fluorophenyl)-1-{4-[(2-piperidyl)ethoxy]benzyl}-1,2,3,4-tetrahydroisoquinolin-6-ol (0.100 g, 0.2 mmol) in pyridine (0.4 ml) was added methyl sulfonyl chloride (25 μl, 0.32 mmol). After stirring for five hours, solvent was removed and the reaction was basified with aqueous sodium bicarbonate solution. The reaction was extracted with dichloromethane and concentrated. The product was purified by semipreparative HLPC (C-18 column, 10-100% acetonitrile/water with 0.1% trifluoroacetic acid). The acetonitrile was removed from the HPLC fractions containing the desired product. Ethyl acetate was added and the solution neutralized using saturated sodium bicarbonate. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated to provide the title compound (0.0135 g, 13% yield): 1H NMR (CDCl3) 6.7-7.1 (m, 11H), 4.78 (t,1H), 4.1 (t, 3H), 3.45-3.62 (m, 2H), 2.62-3.18 (m, 8H), 2.58 (m, 4H), 1.63 (m, 4H), 1.43 (m, 2H); ES−MS (m/z) 539 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686351B2
Source datasetuspto-grants-2004_02
ORD IDord-d892629ef7ec4c7293d4b5c4aa16c6c3
Source noteuspto-grants-2004_02