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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331078Generated: October 30, 2026

Diisopropylethylamine → HCID 59333959, compound

https://huagongshe.com/reaction/331078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Fluoro-1-methyl-4-piperidinecarbonyl chlorideHCID 21050390—
ReactantHCID 68595875HCID 68595875—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59333959HCID 59333959—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 3-[(2-ethoxy-5-fluoropyrimidin-4-yl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate dihydrochloride (120 mg, 0.27 mmol) in 15 mL THF containing diisopropylethyl amine (0.23 mL, 4 eq) was added a 5 mL THF suspension of 4-fluoro-1-methylpiperidine-4-carbonyl chloride (128 mg, 2.6 eq). After heating for 5 hours at 65° C., the reaction was concentrated to dryness and carried on without further purification. To a solution of ethyl 3-[(2-ethoxy-5-fluoropyrimidin-4-yl)amino]-5-[(4-fluoro-1-methylpiperidin-4-yl)carbonyl]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate in methanol was added 2 mL of a 10% sodium hydroxide solution in methanol. After removing the solvent in vacuo, the residue was purified as in Example K1 above. See Table 1 below for NMR data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877761B2
Source datasetuspto-grants-2014_11
ORD IDord-8cfbbd3c40a3480c9699f8f094bfd9ef
Source noteuspto-grants-2014_11