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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451899Generated: October 26, 2026

4-Chloro-7-methoxy-quinazoline → 1,2,3,4-Tetrahydro-3-[1-(7-methoxy-4-quinazolinyl)-4-piperidinyl]-1,6-dimethyl-2,4-dioxoquinazoline

https://huagongshe.com/reaction/1451899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-methoxy-quinazolineHCID 18925078—
Reactant1,2,3,4-Tetrahydro-1,6-dimethyl-2,4-dioxo-3-(4-piperidinyl)quinazoline hydrobromideHCID 21851222—
Product1,2,3,4-Tetrahydro-3-[1-(7-methoxy-4-quinazolinyl)-4-piperidinyl]-1,6-dimethyl-2,4-dioxoquinazolineHCID 2292340822%

Reaction Steps

The procedure similar to that described in Example 57 was repeated, except that 354.0 g (1.0 mmol) of 1,2,3,4-tetrahydro-1,6-dimethyl-2,4-dioxo-3-(4-piperidinyl)quinazoline hydrobromide (Compound v) obtained in Example 41 was used and 4-chloro-7-methoxyquinazoline was used in place of 4-chloro-6,7-dimethoxyquinazoline. As a result, 96.2 mg (yield: 22%) of Compound 85 was obtained as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605900
Source datasetuspto-grants-1997_02
ORD IDord-e9fcbf1d3d4344d98e48f6b72893d511
Source noteuspto-grants-1997_02