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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994836Generated: October 27, 2026

Pyridine-2-sulfonyl Chloride → ethyl 5-(3-methoxypropoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-sulfonyl ChlorideHCID 3787675—
Reactantethyl 7-amino-5-(3-methoxypropoxy)-1H-indole-2-carboxylateHCID 57476210—
SolventPyridineHCID 1049—
Productethyl 5-(3-methoxypropoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylateHCID 5747621290.4%

Reaction Steps

To a mixture of ethyl 7-amino-5-(3-methoxypropoxy)-1H-indole-2-carboxylate (3.00 g) and pyridine (50 mL) was added pyridine-2-sulfonyl chloride (2.0 g) at 0° C., and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated, 1N hydrochloric acid and ethyl acetate were added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed successively with water and saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography, and eluted with hexane-ethyl acetate (2:1-1:1, volume ratio) to give the title compound (4.02 g, yield 90%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane to give colorless prism crystals. melting point 126-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-52f977e7be164144913c2e78b89900d6
Source noteuspto-grants-2010_01