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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765621Generated: October 26, 2026

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

https://huagongshe.com/reaction/1765621

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 numberUS07226929B2
Source datasetuspto-grants-2007_06
ORD IDord-645bc77616c64544bf73d7e4224de4aa
Source noteuspto-grants-2007_06