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HRID 1758381作成日:2026年10月25日

Hydrochloric Acid → 2-(2-Formamidothiazol-4-yl)-2-(2-tert-butoxycarbonylaminoethoxyimino)acetic acid

https://huagongshe.com/reaction/1758381

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
反応物Sodium BicarbonateHCID 516892—
反応物2-(2-Aminoethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acidHCID 54376671—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物2-(2-Formamidothiazol-4-yl)-2-(2-tert-butoxycarbonylaminoethoxyimino)acetic acidHCID 5408288536%

反応手順

A mixture of 2-(2-formamidothiazol-4-yl)-2-(2-aminoethoxyimino)acetic acid (syn isomer, 0.80 g.) and triethylamine (0.45 g.), in a solution of a saturated aqueous solution of sodium bicarbonate (4 ml.), tetrahydrofuran (35 ml.) and water (25 ml.) was adjusted to pH 8.5 with hydrochloric acid. 2-Phenyl-2-(tert-butoxycarbonyloxyimino)acetonitrile (0.77 g.) was added to the stirred solution and stirred at room temperature for 3 hours. After distilling off tetrahydrofuran from the resultant solution, the aqueous solution was washed with diethyl ether, and adjusted to pH 1.5 with 85% phosphoric acid. The solution was extracted with ethyl acetate (50 ml.), and the extract was washed with a saturated aqueous solution of sodium chloride (10 ml.), dried over magnesium sulfate and concentrated under reduced pressure to give 2-(2-formamidothiazol-4-yl)-2-(2-tert-butoxycarbonylaminoethoxyimino)acetic acid (syn isomer, 0.40 g.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04372952
出典データセットuspto-grants-1983_02
ORD IDord-1f0fa2ec43074748a4f7e7094d4a5038
出典メモuspto-grants-1983_02