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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990685Generated: October 26, 2026

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

https://huagongshe.com/reaction/1990685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Alanine 1,1-dimethylethyl esterHCID 89016—
SolventDimethylformamideHCID 6228—
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)propyol]-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 numberUS07645338B2
Source datasetuspto-grants-2010_01
ORD IDord-5193d548512e4a4b923864d7b0df0117
Source noteuspto-grants-2010_01