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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453599Generated: November 2, 2026

Ammonium Chloride → HCID 24880713, compound

https://huagongshe.com/reaction/453599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 59411380HCID 59411380—
SolventEthanolHCID 702—
ProductHCID 24880713HCID 248807130.1%

Reaction Steps

To a solution (150 mL) of sodium ethoxide (7.8 g) in ethanol was added dropwise a mixture of N-(1-benzyl-5-formyl-1H-pyrrol-3-yl)-N-methylthiophene-2-sulfonamide (10.3 g) and ethyl azidoacetate (15 g) under ice-cooling. After the completion of the dropwise addition, the mixture was stirred for 2 hr. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was concentrated. The obtained residue was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:1, volume ratio). The obtained yellow oil was dissolved in toluene (50 mL), and the mixture was stirred at 110° C. for 1 hr. The reaction mixture was concentrated, and the residue was subjected to silica gel column chromatography, eluted with ethyl acetate-hexane (1:1, volume ratio) and concentrated to give ethyl 4-benzyl-6-[methyl(2-thienylsulfonyl)amino]-1,4-dihydropyrrolo[3,2-b]pyrrole-2-carboxylate (13 mg, yield 0.1%) as colorless crystals. melting point 120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492405B2
Source datasetuspto-grants-2013_07
ORD IDord-1a9352807c9742098df01a3158791c65
Source noteuspto-grants-2013_07