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HRID 1198449作成日:2026年10月27日

Ethyl Acetate → (R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1198449

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物2-(4-chlorophenyl)-3,4-dihydro2H-1,4-benzothiazineHCID 13071524—
反応物(S)-N-(2-naphthalenesulfonyl)prolyl chlorideHCID 13576782—
溶媒PyridineHCID 1049—
生成物(R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazineHCID 5424970751.5%

反応手順

To a solution of (±)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (10.01 g, 0.038 mole) in pyridine (150 ml) is added (S)-N-(2-naphthalenesulfonyl)prolyl chloride (18.57 g, 0.057 mole), and the mixture is stirred at room temperature for 4 hours. To the reaction mixture is added ethyl acetate, and the mixture is washed with 5% hydrochloric acid, water, aqueous sodium hydrogen carbonate solution, water and saline in this order, and the ethyl acetate layer is separated, dried over sodium sulfate and distilled to remove the solvent. The resulting caramel is subjected to silica gel column chromatography (hexane:ethyl acetate=5:1-3:1). From the fraction eluted first there is obtained (R)-2-(4-chlorophenyl)-4-[(S)-N-(2-naphthalenesulfonyl)prolyl]-3,4-dihydro 2H-1,4-benzothiazine (10.75 g, 51%) as crystals. M.p. 147°-151° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05281592
出典データセットuspto-grants-1994_01
ORD IDord-a427929280924b28afd13503d52d2f11
出典メモuspto-grants-1994_01