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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353427Generated: November 1, 2026

Benzyl chloroformate → HCID 86635438, compound

https://huagongshe.com/reaction/2353427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylateHCID 11333571—
SolventDichloromethaneHCID 6344—
ProductHCID 86635438HCID 86635438—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the product from Step A (133 mg) in dichloromethane (3 mL) at 0° C. was added N,N-diisopropylethylamine (0.21 mL) followed by benzyl chloroformate (0.1 mL). The reaction mixture was stirred at 0° C. for 90 min, then diluted with dichloromethane (10 mL) and poured into saturated aqueous sodium bicarbonate solution. The layers were separated and the aqueous phase extracted with dichloromethane (3×10 mL). The combined organic phases were dried over anhydrous sodium sulfate, filtered and evaporated in vacuo. The residue was purified on a Biotage Horizon® system (silica gel, 0 to 80% ethyl acetate/hexanes gradient) to give the title compound. LC/MS 359.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750034B2
Source datasetuspto-grants-2010_07
ORD IDord-1a1d89eef63c47a58b020581e2c05d26
Source noteuspto-grants-2010_07