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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062214Generated: November 2, 2026

HCID 67098757, compound → HCID 136121409, compound

https://huagongshe.com/reaction/2062214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67098757HCID 67098757—
Reactant2-(4-Chloro-6-fluoroquinazolin-2-yl)phenolHCID 136121435—
SolventDichloromethaneHCID 6344—
ProductHCID 136121409HCID 13612140991.5%

Reaction Steps

To a mixture of 2-(4-chloro-6-fluoroquinazolin-2-yl)phenol (200 mg, 0.72 mmol) and CH2Cl2 (7 mL) was added (R)-2-hydroxy-4-methyl-1-(piperazin-1-yl)pentan-1-one oxalate (275 mg, 0.95 mmol). The reaction was complete after two hours. Purification via silica gel chromatography using 0-10% EtOAc in 50:50 mixture of CH2Cl2:hexanes gave (R)-1-(4-(6-fluoro-2-(2-hydroxyphenyl)quinazolin-4-yl)piperazin-1-yl)-2-hydroxy-4-methylpentan-1-one (289 mg, 91%). LC/MS: m/z 439.30 (M+H)+ at 3.00 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)). 1H NMR (400 MHz, DMSO-d6) δ 8.46 (m, 1H), 8.02 (m, 1H), 7.84 (m, 2H), 7.40 (m, 1H), 6.97 (m, 2H), 4.92 (d, J=7.2 Hz, 1H), 4.38 (m, 1H), 3.98 (m, 4H), 3.76 (m, 4H), 1.80 (m, 1H), 1.42 (m, 2H), 0.92 (q, J=3.8 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283354B2
Source datasetuspto-grants-2012_10
ORD IDord-4da4267184184e1bbbb511b59d247747
Source noteuspto-grants-2012_10