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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089918생성일: 2026년 10월 26일

Sodium Iodide → 10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline

https://huagongshe.com/reaction/1089918

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물p-Toluenesulfonic acidHCID 6101—
반응물ChlorotrimethylsilaneHCID 6397—
반응물HexamethyldisilazaneHCID 13838—
반응물N,N-Diethyl-1,3-propanediamineHCID 61011—
반응물10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolineHCID 11021716—
용매AcetonitrileHCID 6342—
생성물10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05079363
출처 데이터셋uspto-grants-1992_01
ORD IDord-e86c1c5b169b4ebeb61e406073a700ff
출처 메모uspto-grants-1992_01