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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432970Generated: November 2, 2026

1,1'-Carbonyldiimidazole → 4-(4-Amino-quinazolin-7-ylmethyl)-3-oxo-piperazine-1-carboxylic acid 5-chloro-thiophen-2-ylmethyl ester

https://huagongshe.com/reaction/1432970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(5-Chlorothiophen-2-yl)methanolHCID 12554178—
Reactant1-(4-Aminoquinazoline-7-ylmethyl)piperazine-2-oneHCID 17985174—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventMethanol--water (1/1)HCID 22242641—
Product4-(4-Amino-quinazolin-7-ylmethyl)-3-oxo-piperazine-1-carboxylic acid 5-chloro-thiophen-2-ylmethyl esterHCID 54168402—

Reaction Steps

To a solution of 5-chloro-2-thiophene-methanol (0.10 g, 0.67 mmol, prepared by NaBH4 reduction of 5-chloro-2-thiophene-carboxaldehyde) in 6 mL of CH2Cl2 is added 1,1′-carbonyldiimidazole (0.11 g, 0.67 mmol). The mixture is stirred at room temperature for 3 hours. Then 1-(4-aminoquinazoline-7-ylmethyl)piperazine-2-one (0.17 g, 0.67 mmol, EXAMPLE 72) and a catalytic amount of DMAP is added to the solution and the resulting mixture is heated at 35° C. for 18 hours. The mixture is dissolved in water/MeOH and the crude product is purified by RP-HPLC eluting in a gradient of 10% CH3CN/H2O (0.1% TFA) to 100% CH3CN. The appropriate fractions are combined and lyoppholized to provide the title compound as a white solid. ESI MS, [M+H]+=432,434 (Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-9adc40a79db74eb884011a7a4f14d6d2
Source noteuspto-grants-2009_11