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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868463Generated: October 30, 2026

Benzyl Alcohol → Benzyl 6-((tert-butoxycarbonyl)methyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carbamate

https://huagongshe.com/reaction/1868463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant6-((Tert-butoxycarbonyl)methyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carboxylic acidHCID 67021550—
SolventTolueneHCID 1140—
ProductBenzyl 6-((tert-butoxycarbonyl)methyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carbamateHCID 6702149952.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 6-((tert-butoxycarbonyl)methyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carboxylic acid (Example 58, Step 2, 30 mg, 0.07 mmol) in PhCH3 (3 mL) was added DPPA (19 μL, 0.09 mmol), PhCH2OH (17 μL, 0.17 mmol) and Et3N (12 μL, 0.09 mmol). The reaction was heated to 100° C. for 16 h and was concentrated under reduced pressure. The resulting residue was diluted with EtOAc and extracted with satd aq NH4Cl, NaHCO3 and brine prior to drying over anhydrous MgSO4. Filtration, concentration under reduced pressure and purification by silica gel chromatography afforded benzyl 6-((tert-butoxycarbonyl)methyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carbamate (20 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635699B2
Source datasetuspto-grants-2009_12
ORD IDord-e56a7c52264b4978a986ea9184e0cba8
Source noteuspto-grants-2009_12