HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453599Generated: November 2, 2026
Ammonium Chloride → HCID 24880713, compound
https://huagongshe.com/reaction/453599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 59411380 | HCID 59411380 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24880713 | HCID 24880713 | 0.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492405B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-1a9352807c9742098df01a3158791c65 |
|---|
| Source note | uspto-grants-2013_07 |
|---|