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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357732Generated: October 27, 2026

Formaldehyde → Chloromethyl 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoate

https://huagongshe.com/reaction/2357732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDichloromethaneHCID 6344—
Reactant5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chlorideHCID 86613432—
ProductChloromethyl 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoateHCID 14421522—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chloride (13) (0.040 mole) and paraformaldehyde (0.040 mole) is heated in a sealed vessel at 90° C. for 3 hours. The reaction is cooled, and the solids is dissolved in dichloromethane. The solution is washed with 5% aqueous sodium bicarbonate, with water, and then with a saturated sodium chloride solution. The organic layer is dried over sodium sulfate, filtered and concentrated in vacuo to give crude product, which may be purified by column chromatography on silica gel with hexanes/ethyl acetate as eluent. The fractions that contain pure product may be combined and spin evaporated in vacuo to give chloromethyl 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoate (15). See eg., Bodor, et al., J. Med. Chem., (1980) 23: 469, and Ulich et al., J. Am. Chem. Soc., (1921) 43: 660.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763612B2
Source datasetuspto-grants-2010_07
ORD IDord-9c889689048b49b79d040728ff0dd63a
Source noteuspto-grants-2010_07