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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722401Generated: October 31, 2026

Benzene → 1,6-Dihydro-2-methoxy-4-methyl-6-(3-nitrophenyl)-1-[[(phenylmethyl)amino]carbonyl]-5-pyrimidinecarboxylic acid, 1-methylethyl ester

https://huagongshe.com/reaction/1722401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium ChlorideHCID 5234—
ReactantPhosgeneHCID 6371—
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactant1,4-Dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methyethyl esterHCID 14627197—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1,6-Dihydro-2-methoxy-4-methyl-6-(3-nitrophenyl)-1-[[(phenylmethyl)amino]carbonyl]-5-pyrimidinecarboxylic acid, 1-methylethyl esterHCID 14855106—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1,4-dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methylethyl ester (5.00 g, 15.0 mmol; see Example 2A) and dry triethylamine (6.27 ml, 45 mmol) in dichloromethane (45 ml) in an ice bath under argon was treated with a 1.2M solution of phosgene in benzene (15.0 ml, 18.0 mmol) via syringe. After stirring 4.0 hours at 0° C., the reaction was treated with benzyl amine (2.46 ml, 22.5 mmol) and stirred at ambient temperature overnight. The reaction was treated with water and saturated sodium chloride. The organic phase was evaporated and flash chromatographed (3% ethyl acetate in dichloromethane) to give the title compound as a yellow foam (6.20 g) TLC (5% ethyl acetate/dichlorolmethane) major spot, Rf =0.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855301
Source datasetuspto-grants-1989_08
ORD IDord-9ff8d6bdff9f46049dac2c5f377ec371
Source noteuspto-grants-1989_08