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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620175Generated: October 29, 2026

(+-)-Methionine → HCID 14424031, compound

https://huagongshe.com/reaction/620175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-MethionineHCID 876—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14424030HCID 14424030—
SolventMethanesulfonic AcidHCID 6395—
ProductHCID 14424031HCID 1442403161.9%

Reaction Steps

A mixture of 1.5 g of thienotriazolodiazepine compound obtained in Example 4 and 5 g of DL-methionine in 100 ml of methanesulfonic acid is allowed to stand at room temperature for 24 hours. The mixture is poured into 300 ml of ice-water, neutrarized with an aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic layer is washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After separating by filtration, the filtrate is concentrated to precipitate colorless crystals. The crystals are collected by filtration, washed with isopropyl ether and dried to give 0.9 g of 4-(2-chlorophenyl)-2-[2-(4-hydroxyphenyl)ethyl]-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine, melting at 100°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820703
Source datasetuspto-grants-1989_04
ORD IDord-585556d9f0354fa69cbcf81038a35075
Source noteuspto-grants-1989_04