Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → 4-Benzyloxy-3-aminocarbonylindole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Chlorosulfonyl isocyanate | HCID 70918 | — |
| 반응물 | 4-(phenylmethoxy)-1H-indole | HCID 88465 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Benzyloxy-3-aminocarbonylindole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04442295 |
| 출처 데이터셋 | uspto-grants-1984_04 |
| ORD ID | ord-9ceef1eb7c5944b4af50cf9f5f9483cf |
| 출처 메모 | uspto-grants-1984_04 |