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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283930Generated: November 2, 2026

Triethylamine → HCID 57717538, compound

https://huagongshe.com/reaction/2283930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2-methyl-1-(2-methylpropyl)-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 66958602—
SolventDichloromethaneHCID 6344—
ProductHCID 57717538HCID 5771753846.7%

Reaction Conditions

Temperature4 °C

Reaction Steps

Triethylamine (0.49 mL, 3.53 mmol) was added to a suspension of 2-methyl-1-(2-methylpropyl)-2H-pyrazolo[3,4-c]quinolin-4-amine (prepared as described in Example 3) (0.75 g, 2.95 mmol) in dichloromethane (30 mL) and cooled to 4° C. Ethyl chloroformate (0.352 g, 3.24 mmol) was added in dichloromethane (5 mL) dropwise over 5 minutes to the reaction mixture and maintained at ambient temperature for 16 hours. The reaction mixture was diluted with dichloromethane (25 mL) and washed sequentially with water (25 mL), 4% sodium bicarbonate (2×25 mL), water (25 mL), and brine (25 mL). The combined organic layers were concentrated under reduced pressure and the residue was purified via column chromatography on silica gel (80 g, eluting with 0-10% CMA/chloroform), concentrated under reduced pressure, and recrystallized from diethyl ether to afford 0.45 g of ethyl 1-isobutyl-2-methyl-2H-pyrazolo[3,4-c]quinolin-4-ylcarbamate as white crystals, mp 120-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-f9107e41543f425a9219b81a0cdff95e
Source noteuspto-grants-2015_09