Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469729Generated: October 25, 2026

Diisopropylethylamine → N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine

https://huagongshe.com/reaction/1469729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(4,4-Difluorocyclohexyl)amineHCID 3847030—
Reactant4-Chloro-8-nitroquinazolineHCID 11458471—
SolventIsopropanolHCID 3776—
ProductN-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amineHCID 7167805061.2%

Reaction Steps

A solution of 4-chloro-8-nitroquinazoline (Intermediate-7, step 2, 200 mg, 0.954 mmol), 4,4-difluorocyclohexanamine (491 mg, 2.86 mmol) and DIPEA (367 mg, 2.86 mmol) in iPrOH (2 mL) was heated in a sealed tube at 80° C. for 2 h. Then the reaction mixture was quenched with water at rt and was extracted with CHCl3. The organic layer was separated, dried, filtered and concentrated. The concentrate was purified by column chromatography using 3-5% EtOAc in CHCl3 to afford 180 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 8.59-8.55 (m, 2H), 8.43-8.40 (d, J=7.2 Hz, 1H), 8.27-8.25 (d, J=7.8 Hz, 1H), 7.69-7.63 (t, J=7.8 Hz, 1H), 4.41 (m, 1H), 2.26-2.00 (m, 6H), 1.75-1.71 (m, 2H); MS (m/z): 309.18 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006257B2
Source datasetuspto-grants-2015_04
ORD IDord-0921096d044e42d59ec9c1b94892f827
Source noteuspto-grants-2015_04