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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170233Generated: October 27, 2026

3-(4H-1,2,4-Triazol-4-yl)propan-1-ol → 4-[7-(3-[1,2,4]Triazol-4-yl-propoxy)-quinazolin-4-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1170233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4H-1,2,4-Triazol-4-yl)propan-1-olHCID 12888388—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(7-Fluoro-quinazolin-4-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 59551736—
SolventDimethyl SulfoxideHCID 679—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-[7-(3-[1,2,4]Triazol-4-yl-propoxy)-quinazolin-4-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 59551762—

Reaction Steps

A mixture of 4-(7-fluoro-quinazolin-4-yl)-piperidin-1-carboxylic acid tert-butyl ester (31.6 mg, 95.5 μmol), as prepared in Example 12b, 3-[1,2,4]-triazol-4-yl-propan-1-ol (ChemPacific) (12.0 mg, 94.5 μmol), and KOtBu (11.7 mg, 104 μmol) in DME (100 μL) and DMSO (50 μL) was stirred at rt for 1 hr. The resulting homogeneous amber solution was partitioned with DCM (2 mL) and 0.5M sodium phosphate/pH 7 (2 mL). The organic layer was concentrated to provide the crude title compound. LC/MS (ESI): calcd mass 438.2, found 439.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825244B2
Source datasetuspto-grants-2010_11
ORD IDord-5260b5625a224eea928ad8dce196dde1
Source noteuspto-grants-2010_11