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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723324Generated: October 29, 2026

Ethyl chloroformate → 5-tert-Butyl 1-ethyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-1,5-dicarboxylate

https://huagongshe.com/reaction/723324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylateHCID 11333571—
SolventTetrahydrofuranHCID 8028—
Product5-tert-Butyl 1-ethyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-1,5-dicarboxylateHCID 691904572%

Reaction Steps

A solution of ethyl chlorocarbonate (8.9 ml, 93 mmol) in tetrahydrofuran (THF, 250 ml) was slowly added to a mixture of tert-butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (20 g, 89 mmol) and diisopropylethylamine (DIEA, 92 ml, 528 mmol) in THF (500 ml) at 0–5° C. The reaction was kept at the same temperature for two hours then allowed to reach room temperature and stirred overnight. The obtained mixture was evaporated to dryness under vacuum, and the resulting residue extracted with ethyl acetate (AcOEt) and water. The organic layer was separated, dried over sodium sulfate and evaporated to dryness. The mixture was purified by flash-chromatography (eluent: ethyl acetate/cyclohexane 4/6 to 7/3) to give 19 g of the title compound as a white solid. [M+H]+ 297

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141568B2
Source datasetuspto-grants-2006_11
ORD IDord-98e4eae537ed454ab1581bc6a63385b6
Source noteuspto-grants-2006_11