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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079325Generated: November 2, 2026

Hydrochloric Acid → Benzyl 3-(hydroxymethyl)-4-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperazine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/2079325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant3-Hydroxymethyl-4-[2-(2-hydroxy-phenyl)-7-methyl-quinazolin-4-yl]-piperazine-1-carboxylic acid benzyl esterHCID 136121321—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-(hydroxymethyl)-4-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperazine-1-carboxylate hydrochlorideHCID 136366705—

Reaction Steps

A 2.0 M HCl solution in Et2O (212 μL, 0.42 mmol) was slowly added at room temperature to a stirring solution of 3-hydroxymethyl-4-[2-(2-hydroxy-phenyl)-7-methyl-quinazolin-4-yl]-piperazine-1-carboxylic acid benzyl ester (206 mg, 0.42 mmol) in 500 μL of CH2Cl2. The reaction was stirred for 1 hour. Solvents were removed under reduced pressure, and the residue was triturated with Et2O and filtered to give benzyl 3-(hydroxymethyl)-4-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperazine-1-carboxylate hydrochloride. LC/MS: m/z 485.5 (M+H)+ at 3.07 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-a0657bce9b4e4d76b0045d197aa00f51
Source noteuspto-grants-2011_04