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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031247Generated: October 29, 2026

O-methyl-L-tyrosine N-Methylamide → 6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl ester

https://huagongshe.com/reaction/1031247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-methyl-L-tyrosine N-MethylamideHCID 14303038—
Reactant4-Methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acidHCID 53859812—
SolventDichloromethaneHCID 6344—
Product6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl esterHCID 8511523453.3%

Reaction Steps

N,N-Dicyclohexylcarbodiimide (515 mg, 2.5 mmol) was added to an ice-cooled solution of 4-methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acid (500 mg, 2.5 mmol) and O-methyl-L-tyrosine N-methylamide (520 mg, 2.5 mmol) in dry dichloromethane (30 ml), and the mixture was stirred at room temperature for 18 h. The precipitated solid was filtered off and washed with a little dichloromethane, then the organic solution was washed successively with 1 N hydrochloric acid (20 ml), 1 N sodium bicarbonate (20 ml), and water. The solution was dried (MgSO4) and evaporated in vacuo. Column chromatography (30 g silica) of the residual solid, eluting with 5% methanol/dichloromethane gave the title compound (520 mg, 53%), m.p. 142°-144° C. (dichloromethane/pentane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05109000
Source datasetuspto-grants-1992_04
ORD IDord-9850084518aa4b078e4f5093254fa10a
Source noteuspto-grants-1992_04