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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353465Generated: October 31, 2026

Ethanesulfonyl chloride → HCID 68425037, compound

https://huagongshe.com/reaction/2353465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant6-Bromo-1,2,3,4-tetrahydroquinolineHCID 4715029—
ProductHCID 68425037HCID 6842503736.5%

Reaction Steps

This compound was prepared according to the general procedure for sulfonylation of indolines and tetrahydroquinolines described in Example 4 using 6-bromo-1,2,3,4-tetrahydroquinoline (0.40 g, 1.89 mmol) and ethanesulfonyl chloride (0.26 mL, 2.8 mmol) to provide 6-bromo-1-(ethylsulfonyl)-1,2,3,4-tetrahydroquinoline (0.21 g). MS (ES) m/z 303.7; HPLC purity 94.8% at 210-370 nm, 9.6 min.; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammonium formate buffer pH=3.5 acetonitrile+MeOH) for 10 minutes, hold 4 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750038B2
Source datasetuspto-grants-2010_07
ORD IDord-d7fc095ea4284bac93dcb910ebe42ce2
Source noteuspto-grants-2010_07