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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782252Generated: October 26, 2026

Methanamine, hydrochloride (1:1) → 1-[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine

https://huagongshe.com/reaction/1782252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, hydrochloride (1:1)HCID 11637—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 86232805—
SolventMethanolHCID 887—
Product1-[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamineHCID 66924663120%

Reaction Steps

To a solution (60 mL) of 5-bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde (3.5 g) in methanol were added methylammonium chloride (7.5 g) and sodium cyanoborohydride (2.4 g), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, saturated aqueous sodium hydrogencarbonate solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound as a brown oil (yield 4.4 g, about 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498337B2
Source datasetuspto-grants-2009_03
ORD IDord-7cb62c60d9c9462399bccfcb0b15408b
Source noteuspto-grants-2009_03