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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469730Generated: October 25, 2026

Ammonium Chloride → N4-(4,4-difluorocyclohexyl)quinazoline-4,8-diamine

https://huagongshe.com/reaction/1469730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amineHCID 71678050—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductN4-(4,4-difluorocyclohexyl)quinazoline-4,8-diamineHCID 8669223086.1%

Reaction Steps

To a solution of N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine (90 mg, 0.292 mmol) in EtOH (2 mL) were added iron powder (163 mg, 2.92 mmol) and NH4Cl (127 mg, 2.33 mmol) and the reaction mixture was heated at reflux for 2 h. Then the reaction mixture was filtered through celite. The celite bed was washed with 10% MeOH in CHCl3. The filtrate was washed with a saturated aq. NaHCO3 solution and water. The organic layer was separated, dried, filtered and concentrated to afford 70 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 8.38 (s, 1H), 7.64 (d, J=7.2 Hz, 1H), 7.35 (d, J=7.8 Hz, 1H), 7.19-7.14 (t, J=7.8 Hz, 1H), 6.87 (d, J=7.8 Hz, 1H), 5.71 (s, 2H), 4.38 (m, 1H), 2.09-1.97 (m, 6H), 1.73-1.69 (m, 2H); MS (m/z): 279.12 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006257B2
Source datasetuspto-grants-2015_04
ORD IDord-c9003f49b274484295f2f9369bcce0e5
Source noteuspto-grants-2015_04