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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237163Generated: November 2, 2026

Di-tert-butyl dicarbonate → Tert-butyl 6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-ylcarbamate

https://huagongshe.com/reaction/2237163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-Amino-6-(2-fluoro-4-nitrophenoxy)pyrimidineHCID 23153012—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-ylcarbamateHCID 5985292126.2%

Reaction Steps

A mixture of 6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-amine (439 mg, 1.2 mmol), BOC2O (261 mg, 1.2 mmol), DMAP (10 mg), and THF (10 mL) was stirred at RT for 1 h then concentrated in vacuo to give the crude product. The product was purified by flash chromatography using 1-2% MeOH in CH2Cl2 as the eluent to give tert-butyl 6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-ylcarbamate as a white solid (110 mg, 26%). 1H NMR (DMSO-d6) δ 10.59 (s, 1H), 8.39 (dd, 1H, J=8.8, 1.1 Hz), 8.32 (dd, 1H, J=10.3, 2.4 Hz), 8.15 (ddd, 1H, J=9.1, 2.5, 1.0 Hz), 7.67 (dd, 1H, J=8.8, 8.8 Hz), 7.45 (s, 1H), 1.44 (s, 9H); MS(ESI−) m/z 349.08 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-ebc1de02d6d14290a3ab01a6cb28c751
Source noteuspto-grants-2010_05