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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735341Generated: October 30, 2026

Triethylamine → 2,4-Di[(1,1-dimethylethyl)carbonylamino]-6-(3-trifluoromethylphenylmethoxyimino)-5,6,7,8-tetrahydroquinazoline

https://huagongshe.com/reaction/1735341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-((3-(Trifluoromethyl)phenyl)methyl)hydroxylamine--hydrogen chloride (1/1)HCID 203812—
Reactant2,4-Di[(1,1-dimethylethyl)carbonylamino]-5,6,7,8-tetrahydro-6-quinazolinoneHCID 19705190—
SolventEthanolHCID 702—
Product2,4-Di[(1,1-dimethylethyl)carbonylamino]-6-(3-trifluoromethylphenylmethoxyimino)-5,6,7,8-tetrahydroquinazolineHCID 54231774—

Reaction Steps

This compound is prepared in a manner analogous to that of Step E of Example 12, using 3.5 grams (0.010 mole) of 2,4-di[(1,1-dimethylethyl)carbonylamino]-5,6,7,8-tetrahydro-6-quinazolinone (prepared in Step C of Example 12) and 2.7 grams (0.012 mole) of O-(3-trifluoromethylphenylmethyl)hydroxylamine hydrochloride in about 45 mL of ethanol. This preparation differs from Step E of Example 12 in that prior to heating at reflux for four hours, 1.5 grams (0.015 mole) of triethylamine is added as an acid acceptor, yielding 2,4-di[(1,1-dimethylethyl)carbonylamino]-6-(3-trifluoromethylphenylmethoxyimino)-5,6,7,8-tetrahydroquinazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536725
Source datasetuspto-grants-1996_07
ORD IDord-060d0c4541864ec9b7f6528dae2806c5
Source noteuspto-grants-1996_07