Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Iodide → 10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Hexamethyldisilazane | HCID 13838 | — |
| 반응물 | N,N-Diethyl-1,3-propanediamine | HCID 61011 | — |
| 반응물 | 10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline | HCID 11021716 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline | HCID 57067349 | — |
반응 단계
0.87 g (0.0033 mole) of 10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline and 0.495 g (0.003 mole) of sodium iodide are suspended in 25 ml of acetonitrile and 4.2 ml (0.33 mole) of trimethylsilylchloride, and then heated at 40° C. for 17 hours. 10.5 ml (0.050 mole) of hexamethyldisilazane, 0.113 g (6×10-4 mole) of anhydrous p-toluenesulfonic acid and 22.4 ml (0.14 mole) of diethylaminopropylamine are then added. After distillation of the acetonitrile, the mixture is heated at reflux for 20 hours. It is evaporated to dryness under a partial vacuum and the residue is stirred with 20 ml of water and 5 ml of diisopropyl ether for 1 hour. The precipitate obtained is filtered off and dried under vacuum at 50° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05079363 |
| 출처 데이터셋 | uspto-grants-1992_01 |
| ORD ID | ord-e86c1c5b169b4ebeb61e406073a700ff |
| 출처 메모 | uspto-grants-1992_01 |