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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7272Generated: October 26, 2026

L-Methionine → tert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninate

https://huagongshe.com/reaction/7272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Alanine 1,1-dimethylethyl esterHCID 89016—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Producttert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninateHCID 16124765109.3%

Reaction Steps

Z-Protected L-methionine (10 g) was dissolved in DMF (200 ml) and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (8.13 g) was added followed by HOBT (5.72 g) and triethylamine (19.7 ml). The mixture was stirred for 1 h then L-alanine tert-butyl ester (7.7 g) was added and stirring continued for 18 h. The mixture was concentrated under reduced pressure and partitioned between diethyl ether and water. The separated organic phase was washed with hydrochloric acid (1M), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (11.9 g) as an orange oil which crystallised on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084139B2
Source datasetuspto-grants-2006_08
ORD IDord-acb43fa5eb1b42d09e33b5d59c24f091
Source noteuspto-grants-2006_08