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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066172Generated: November 1, 2026

tert-Butanol → Tert-butyl [4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridin-2-yl]carbamate

https://huagongshe.com/reaction/2066172

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-(4-Benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylic acidHCID 23153098—
ProductTert-butyl [4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridin-2-yl]carbamateHCID 5767735565.5%

Reaction Steps

To a suspension of 4-(4-benzyloxycarbonylamino-3-fluorophenoxy)pyridine-2-carboxylic acid (5.04 g) in tert-butanol (50 ml) was added triethylamine (4.6 ml) at room temperature, followed by stirring. Diphenylphosphoryl azide (3.13 ml) was added thereto at room temperature, followed by stirring under a nitrogen atmosphere at room temperature for 30 min. Then the reaction mixture was heated and stirred at 90° C. for 30 min and at 100° C. for 4 hr. The reaction mixture was allowed to cool down to room temperature. Ethyl acetate (25 ml) was added thereto, and the reaction mixture was stirred in an ice bath for 30 min. Precipitated crystals were collected by filtration and washed with diethyl ether. These crystals were dried under aeration at room temperature for 1 hr to provide the titled compound as colorless crystals (3.92 g, 65.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288538B2
Source datasetuspto-grants-2012_10
ORD IDord-641ed045bf004a5bafac179b7340bc9d
Source noteuspto-grants-2012_10