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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606428Generated: October 30, 2026

Methanol → N-{[3'-({[(4-oxo-3,4-dihydroquinazolin-2-yl)carbonyl]amino}methyl)biphenyl-4-yl]sulfonyl}valine

https://huagongshe.com/reaction/606428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl N-{[3'-({[(4-oxo-3,4-dihydroquinazolin-2-yl)carbonyl]amino}methyl)biphenyl-4-yl]sulfonyl}valinateHCID 136380956—
SolventTetrahydrofuranHCID 8028—
ProductN-{[3'-({[(4-oxo-3,4-dihydroquinazolin-2-yl)carbonyl]amino}methyl)biphenyl-4-yl]sulfonyl}valineHCID 13638095883%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of methyl N-{[3′-({[(4-oxo-3,4-dihydroquinazolin-2-yl)carbonyl]amino}methyl)biphenyl-4-yl]sulfonyl}valinate obtained in Reference Example 95 (0.250 g, 0.456 mmol) in THF (3 mL)-methanol (3 mL)-water (3 mL) was added 4N aqueous sodium hydroxide solution (0.399 mL, 1.60 mmol) at room temperature, and the mixture was stirred under heating at 80° C. for 15 hr. The reaction mixture was allowed to cool to room temperature, and concentrated under reduced pressure, and the residue was diluted with water. The mixture was acidified with 1N hydrochloric acid, and partitioned between ethyl acetate and water. The organic layer was washed with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized from methanol to give the title compound as a white powder (0.202 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915267B2
Source datasetuspto-grants-2011_03
ORD IDord-d20f1c67d5b64deb9eece31ac70cb754
Source noteuspto-grants-2011_03