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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325766생성일: 2026년 10월 27일

Acetonitrile → 4-Benzyloxy-3-aminocarbonylindole

https://huagongshe.com/reaction/325766

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium HydroxideHCID 14797—
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물4-(phenylmethoxy)-1H-indoleHCID 88465—
용매WaterHCID 962—
생성물4-Benzyloxy-3-aminocarbonylindoleHCID 12798009—

반응 단계

4.4 g. 4-Benzyloxyindole (see Helv. Chim. Acta, 54. 2411/1971) are dissolved in 20 ml. anhydrous acetonitrile, cooled to 0° C. and mixed with 1.8 ml. N-carbonylsulphamoyl chloride in 20 ml. acetonitrile. After a reaction period of about 1 hour, a solution of 3.4 g. potassium hydroxide in 34 ml. water is added thereto and the reaction mixture then stirred for 1 hour at ambient temperature. After evaporating the solvent, the residue is taken up in 200 ml. 2 N hydrochloric acid and extracted with methylene chloride. From the methylene chloride extract there are obtained 4.8 g. (45% of theory) 4-benzyloxy-3-aminocarbonylindole, which is recrystallized from ethyl acetate; m.p. 176° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04442295
출처 데이터셋uspto-grants-1984_04
ORD IDord-9ceef1eb7c5944b4af50cf9f5f9483cf
출처 메모uspto-grants-1984_04