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HRID 255749생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/255749

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
반응물Sodium BicarbonateHCID 516892—
반응물2-(2-Aminoethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acidHCID 54376671—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물2-(2-Formamidothiazol-4-yl)-2-(2-tert-butoxycarbonylaminoethoxyimino)acetic acidHCID 5408288536%

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04698337
출처 데이터셋uspto-grants-1987_10
ORD IDord-37fd78a4d11f4f47909d365a6e03a51d
출처 메모uspto-grants-1987_10