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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7629Generated: October 25, 2026

Tetrahydrofuran → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/reaction/7629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acidHCID 21991771—
Reactant4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl esterHCID 69594337—
Reactant4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) esterHCID 86593646—
SolventWaterHCID 962—
Product2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1002018065%

Reaction Steps

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087612B2
Source datasetuspto-grants-2006_08
ORD IDord-ad3689421b0444ecba177dceb56a6917
Source noteuspto-grants-2006_08