Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360604Generated: October 31, 2026

Triethylamine → HCID 57717569, compound

https://huagongshe.com/reaction/1360604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsopropyl isocyanateHCID 61277—
ReactantHCID 57717585HCID 57717585—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 57717569HCID 57717569—

Reaction Conditions

Temperature4 °C

Reaction Steps

Triethylamine (2.84 mL, 20.4 mmol) was added to a suspension of 1-(2-aminoethyl)-2-methyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-4-amine (prepared as described in Example 50) (1.0 g, 4.08 mmol) in dichloromethane (50 mL) and cooled to 4° C. Isopropyl isocyanate (0.44 mL, 4.48 mmol) was added dropwise to the reaction mixture and maintained at ambient temperature for 16 hours. The reaction mixture was diluted with chloroform (50 mL) and the precipitate was collected by filtration, washed with water, and dried under reduced pressure to afford N-[2-(4-amino-2-methyl-6,7,8,9-tetrahydro-2H-pyrazolo[3,4-c]quinolin-1-yl)ethyl]-N′-isopropylurea as tan needles, mp 237-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-48c4bae090804e1f86980827a07db638
Source noteuspto-grants-2011_02