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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443460Generated: November 2, 2026

17-Hydroxy-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl ester → 17-[2-(4-Fluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid

https://huagongshe.com/reaction/1443460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17-Hydroxy-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl esterHCID 68410372—
ReactantHCID 178487732HCID 178487732—
Product17-[2-(4-Fluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acidHCID 68411340—

Reaction Steps

Quinazolinol derivative (92) (141 mg, 0.5 mmol) was coupled to compound 51 (170 mg, 0.45 mmol) as described in example 52, which gave the crude ethyl ester of the title compound. The crude ester was purified by flash chromatography on silica gel eluted with 5→15% MeOH in diethyl ether, the afforded residue was dissolved in dichloromethane and filtered to remove traces of silica, which gave the ethyl ester of the title compound (135 mg, 46%). The ethyl ester was then hydrolyzed as described in example 52, which gave the title compound (125 mg, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659245B2
Source datasetuspto-grants-2010_02
ORD IDord-6053d68f4f274d6488f10a2958701a08
Source noteuspto-grants-2010_02