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HRID 977215作成日:2026年10月27日

Hydrogen Sulfide → tert-butyl (2R)-2-[3-(4-thiocarbamoylphenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionate

https://huagongshe.com/reaction/977215

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen SulfideHCID 402—
反応物PyridineHCID 1049—
反応物tert-butyl (2R)-2-[3-(4-cyanophenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionateHCID 70116075—
溶媒TriethylamineHCID 8471—
生成物tert-butyl (2R)-2-[3-(4-thiocarbamoylphenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionateHCID 54209529—

反応手順

2.6 g of tert-butyl (2R)-2-[3-(4-cyanophenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionate [obtainable according to Example 8] are dissolved in a solvent mixture consisting of 30 ml of pyridine and 5 ml of triethylamine and the mixture is stirred for 1.5 h with ice cooling, with H2S gas being passed in continuously during this phase. The reaction mixture is subsequently stirred at room temperature for 24 h. Concentration by evaporation and customary workup give tert-butyl (2R)-2-[3-(4-thiocarbamoylphenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionate, m.p. 185°-186°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05614535
出典データセットuspto-grants-1997_03
ORD IDord-47f8fb613651463cab3890f6ad234aee
出典メモuspto-grants-1997_03