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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525237Generated: November 4, 2026

Benzyl Alcohol → Benzyl 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidin-5-ylcarbamate

https://huagongshe.com/reaction/1525237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylic acidHCID 67459483—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidin-5-ylcarbamateHCID 67459577—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-(benzyloxy)-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxylic acid, 11-c, (2 g, 6.76 mmol) in dry THF (40 ml) and toluene (40 ml) were added Et3N (2.04 g, 20.3 mmol), DPPA (2.04 g, 7.43 mmol) and benzyl alcohol (1.1 g, 10.1 mmol). The resulting mixture was heated at 60° C. for 12 hours. The mixture was concentrated under vacuum and the residue was purified on silica gel column with the eluent of ethyl acetate/petroleum ether=1/5 (Rf=0.6) to provide the product, 11-d, (1.96 g, 72.6%). 1H NMR (DMSO-d6, 300 MHz,): δ 9.39 (br, 1H), 8.73 (s, 1H), 8.62 (s, 1H), 7.83 (s, 1H), 7.56 (m, 2H), 7.33 (m, 8H), 6.57 (m, 1H), 5.58 (s, 2H), 5.16 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079930B2
Source datasetuspto-grants-2015_07
ORD IDord-e9dfce5ae92640a9b8928b4ba31e287d
Source noteuspto-grants-2015_07