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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257734Generated: October 26, 2026

7-(Benzyloxy)-4-chloro-6-methoxyquinazoline → 3-[1-(7-Benzyloxy-6-methoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-1,6-dimethyl-2,4-dioxoquinazoline

https://huagongshe.com/reaction/2257734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
Reactant1,2,3,4-Tetrahydro-1,6-dimethyl-2,4-dioxo-3-(4-piperidinyl)quinazoline hydrobromideHCID 21851222—
Product3-[1-(7-Benzyloxy-6-methoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-1,6-dimethyl-2,4-dioxoquinazolineHCID 2292343642%

Reaction Steps

The procedure similar to that described in Example 57 was repeated, except that 369.0 mg (1.05 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 7-benzyloxy-4-chloro-6-methoxyquinazoline was used in place of 4-chloro-6,7-dimethoxyquinazoline. As a result, 233.8 mg (yield: 42%) of Compound 87 was obtained as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658917
Source datasetuspto-grants-1997_08
ORD IDord-e0a61c2dbc20411e82a4a4cf297291df
Source noteuspto-grants-1997_08