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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984045Generated: October 27, 2026

Ethyl 2-amino-3-sulfanylpropanoate → (+/-)-ethyl alpha-[[[(4-chlorophenyl)[2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl]methyl]thio]methyl]glycine

https://huagongshe.com/reaction/984045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-amino-3-sulfanylpropanoateHCID 3297—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodiumHCID 5360545—
Reactant3-chloro-4-[chloro(4-chlorophenyl)methyl]phenyl-1,2,4-triazine-3,5(2H,4H)-dioneHCID 22557357—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-ethyl alpha-[[[(4-chlorophenyl)[2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl]methyl]thio]methyl]glycineHCID 86585301—

Reaction Steps

Sodium (0.075 mol) was added portionwise to ethanol (50 ml) under N2 atmosphere and this mixture was stirred until complete dissolution. Ethyl 2-amino-3-mercaptopropanoate (0.075 mol) was added and the mixture was stirred for 2 hours at RT. The solvent was evaporated, THF (50 ml) was added to the residue, and a solution of 2-[3-chloro-4-[chloro(4-chlorophenyl)methyl]phenyl]-1,2,4-triazine-3,5(2H,4H)-dione (0.015 mol) in THF (50 ml) was added. 1,8-diazabicyclo[5.4.0]undec-7-ene (0.03 mol) was added and the resulting reaction mixture was stirred overnight at RT. The solvent was evaporated. The residue was stirred in water and extracted with CH2Cl2. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. This fraction was purified by HPLC over silica gel (eluent: CH2Cl2/CH2OH 97/3). The pure fractions were collected and the solvent was evaporated. The residue was stirred in DIPE, filtered off, washed and dried, yielding (±)-ethyl α-[[[(4-chlorophenyl)[2-chloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)phenyl]methyl]thio]methyl]glycine (compound 95).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867207B2
Source datasetuspto-grants-2005_03
ORD IDord-35eaf45b7e7e4182bd1df1f11857821c
Source noteuspto-grants-2005_03