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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978061Generated: November 1, 2026

Phenyl isocyanate → HCID 69943240, compound

https://huagongshe.com/reaction/1978061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 69942786HCID 69942786—
SolventDimethylformamideHCID 6228—
ProductHCID 69943240HCID 69943240—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.8 g of 2(R)-[2-amino-1(R)-(tert-butoxycarbonyl)ethyl]-2′-(methanesulphonyl)-4-methyl-2′-phenylvalerohydrazide prepared as described in Example 33, part (i), 0.325 ml of N,N-diisopropylethylamine and 0.21 ml of phenyl isocyanate in 10 ml of dimethylformamide was stirred at 60° C. under nitrogen for 2.5 hours. The solvent was evaporated and the residue was partitioned between ethyl acetate and 1M hydrochloric acid. The ethyl acetate solution was separated and washed with sodium hydrogen carbonate solution and with saturated sodium chloride solution, dried over anhydrous magnesium sulphate and evaporated. The residue was triturated with diethyl ether and there was obtained 0.705 g of 2(R)-[1(R)-(tert-butoxycarbonyl)-2-(3-phenylureido)ethyl]-2′-(methanesulphonyl)-4-methyl-2′-phenylvalerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235787B1
Source datasetuspto-grants-2001_05
ORD IDord-3a057a69bf284350bf1b4460556e9a2f
Source noteuspto-grants-2001_05