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HRID 80278생성일: 2026년 10월 24일

Methanol → 3-(Benzothiazol-6-ylamino)-butyric acid

https://huagongshe.com/ko/reaction/80278

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 3-aminobutyrateHCID 98103—
반응물6-Iodo-1,3-benzothiazoleHCID 22609002—
촉매Copper iodideHCID 83717—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물3-(Benzothiazol-6-ylamino)-butyric acidHCID 5963619122.22%

반응 조건

온도110 °C

반응 단계

3-Amino-butyric acid ethyl ester (2 g, 15.27 mmol), 6-iodo-benzothiazole (3.98 g, 15.27 mmol) and potassium carbonate (5.27 g, 38.18 mmol) were dissolved in DMF (50 mL) and the reaction mixture was purged with argon for 10 minutes. This was followed by the addition of copper iodide (290 mg, 1.527 mmol) and the resulting mixture was heated to 110° C. overnight. The reaction was monitored by TLC (10% MeOH in CHCl3) which showed the presence of starting material. The reaction mixture was heated to 120° C. for a further 24 hours. The reaction mixture was concentrated and adjusted the pH to 5 using acetic acid. The reaction mixture was partitioned between water and ethylacetate. The organic layer was dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (1% MeOH in CHCl3) afforded 800 mg of the product (22.22% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-81561b64d3fa41a6b24658c8cb878a6e
출처 메모uspto-grants-2014_09