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HRID 2179932作成日:2026年10月27日

Ethyl methyl sulfide → 3-Phenyl-2-prop-2-ynylamino-propionic acid methyl ester

https://huagongshe.com/reaction/2179932

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl methyl sulfideHCID 12230—
反応物2-[(4-Methoxy-2,3,6-trimethyl-benzenesulfonyl)-prop-2-ynyl-amino]-3-phenyl-propionic acid methyl esterHCID 20779306—
溶媒1,1-DichloroethaneHCID 6365—
溶媒Trifluoroacetic acidHCID 6422—
生成物3-Phenyl-2-prop-2-ynylamino-propionic acid methyl esterHCID 20779308—

反応手順

To a solution of 2-[(4-Methoxy-2,3,6-trimethyl-benzenesulfonyl)-prop-2-ynyl-amino]-3-phenyl-propionic acid methyl ester (150 mg, 0.349 mmol) in anhydrous dichloroethane (1.5 mL), trifluoroacetic acid (3.5 mL) and ethyl methyl sulfide (0.16 mL, 1.75 mmol) were added. The reaction mixture was stirred at room temperature under a N2 atmosphere for 12 h. Excess of solvents were removed under reduced pressure and the residue was extracted between saturated NaHCO3 solution and ethyl acetate. The organic layer was separated, dried (Na2SO4), concentrated. The crude product was purified by silica gel column chromatography using ethyl acetate and hexane (1:3) as eluent to obtain 3-Phenyl-2-prop-2-ynylamino-propionic acid methyl ester as a thick syrup, 70 mg (92%). 1H NMR (CDCl3, 400 MHz): δ7.32-7.19 (m, 5H), 3.78 (t, 1H), 3.68 (s, 3H), 3.40 (ABq, 2H), 3.03 (dd, 1H), 2.98 (dd, 1H), 1.99 (t, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06887877B2
出典データセットuspto-grants-2005_05
ORD IDord-14d2abf5250847349088d3c5a01ad3f0
出典メモuspto-grants-2005_05