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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466988Generated: October 30, 2026

Water → HCID 178456605, compound

https://huagongshe.com/reaction/466988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-(2-Cyanophenyl)-N'-prop-2-en-1-ylureaHCID 14271357—
SolventEthanolHCID 702—
SolventAzane;hydrateHCID 12896473—
ProductHCID 178456605HCID 17845660584%

Reaction Steps

A mixture of 2-(3-allylureido)benzonitrile (10.0 g, 50 mmol) in ethanol (70 mL) and 28% of ammonia water (50 mL) was heated on a steam bath with occasional stirring for 15 minutes. The mixture was then cooled to room temperature and to the mixture was added water (100 mL). The solid was collected by filtration and was recrystallized from methanol with a few drops of ammonia water to give 8.4 g (84%) of 3,4-dihydro-4-imino-3-allyl-2(1H)-quinazolinone, mp 223°-224° C. IR (KBr): 3284, 3203, 3147, 1691, 1582 cm-1. 1H NMR (300 MHz, DMSO-d6): δ4.61 (d, 2H, =CH2), 5.08 (q, 2H, CH2), 5.85 (m, 1H, =CH), 7.07 (m, 2H, Ar--H), 7.46 (t, 1H, Ar--H), 8.04 (d, 1H, Ar--H), 8.85 (br s, 1H, NH), 10.74 (s, 1H, NH). 13C NMR (75 MHz, DMSO-d6): δ42.54, 115.08, 115.81, 122.09, 126.13, 132.77, 133.15, 137.01, 149.76. Anal. Calcd for C11H11N3O; C, 65.63; H, 5.56; N, 20.87. Found: C, 65.67; H, 5.51; N, 20.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158953
Source datasetuspto-grants-1992_10
ORD IDord-84b9e884a2654fd5a742a3899bd854e8
Source noteuspto-grants-1992_10