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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448272Generated: October 29, 2026

1-Methylpiperazine → HCID 178481079, compound

https://huagongshe.com/reaction/448272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantHCID 68649464HCID 68649464—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 178481079HCID 178481079112.9%

Reaction Steps

To a solution of triphosgene (195 mg, 0.65 mmol, 0.56 eq) in DCM (15 ml) was added a solution of ethyl 3-[(4-fluorobenzoyl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride (442 mg, 1.15 mmol) in DCM (30 ml) followed by N,N-diisopropylethylamine (760 μl, 4.31 mmol, 3.75 eq). After 3 hours, a solution of N-methylpiperazine (195 μl, 1.72 mmol, 1.5 eq) and diisopropylethylamine (300 μl, 1.72 mmol, 1.5 eq) in DCM (8 ml) was added. The reaction was stirred overnight at room temperature (TLC:CH2Cl2/MeOH 90/10). The solution was washed with brine, the organic phase was dried over sodium sulfate and concentrated. The residue was dissolved in methanol (16 ml), treated with TEA (1.6 ml, 11.5 mmol, 10 eq) and stirred overnight at room temperature. (TLC: CH2Cl2/MeOH 90/10). After evaporation, the solid was purified by flash chromatography (eluent: CH2Cl2/MeOH 90/10). The solid was treated with diisopropylether and filtered to afford 0.294 g of the title compound in 64% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481585B2
Source datasetuspto-grants-2013_07
ORD IDord-234b9e540c00419d8f67610c5d1442c2
Source noteuspto-grants-2013_07