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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070410Generated: November 1, 2026

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

https://huagongshe.com/reaction/2070410

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 numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-720cda0aafb0481ba0ab237677582e99
Source noteuspto-grants-2012_10