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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069149Generated: October 30, 2026

2,4-Dichloropyrimidine → tert-Butyl 4-(2-chloropyrimidin-4-yloxy)naphthalen-1-ylcarbamate

https://huagongshe.com/reaction/2069149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactanttert-Butyl (4-hydroxynaphthalen-1-yl)carbamateHCID 10923237—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(2-chloropyrimidin-4-yloxy)naphthalen-1-ylcarbamateHCID 8666049035.7%

Reaction Steps

To a degassed solution of tert-butyl 4-hydroxynaphthalen-1-ylcarbamate (13.3 g, 51.3 mmol) and DBU (12.6 mL, 51.3 mmol) in MeCN (80 mL) under nitrogen was added 2,4-dichloropyrimidine (7.65 g, 51.3 mmol) in acetonitrile (19 mL) and the reaction mixture was heated to reflux for 4 hr. The solvent was evaporated in vacuo and the residue was taken up into DCM (100 mL) and was washed with water (2×100 mL) and brine (100 mL), then dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 330 g, EtOAc in isohexane, 0-50%, gradient elution) to afford the title compound as a pale pink solid (6.80 g, 34%); Rt 2.50 min (Method 2); m/z 372/374 (M+H)+, (ES+)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299074B2
Source datasetuspto-grants-2012_10
ORD IDord-7449f2539e8440288049f9602ea94c3b
Source noteuspto-grants-2012_10