Sodium Iodide → 1-Ethyl-3,3,5-trimethyl-7-[3-(2-phenylpiperidin-1-yl)propoxy]-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione hydrochloride

HRID 1504225

반응식

HRID 1504225 반응식
C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[C:9]1([CH:15]2[CH2:20][CH2:19][CH2:18][CH2:17][NH:16]2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[Cl:21][CH2:22][CH2:23][CH2:24][O:25][C:26]1[CH:43]=[CH:42][C:29]2[N:30]([CH2:40][CH3:41])[C:31](=[O:39])[C:32]([CH3:38])([CH3:37])[C:33](=[O:36])[N:34]([CH3:35])[C:28]=2[CH:27]=1.C(OC(=O)C)C.Cl>C(OCC)(=O)C.O.CN(C=O)C>[ClH:21].[CH2:40]([N:30]1[C:31](=[O:39])[C:32]([CH3:37])([CH3:38])[C:33](=[O:36])[N:34]([CH3:35])[C:28]2[CH:27]=[C:26]([O:25][CH2:24][CH2:23][CH2:22][N:16]3[CH2:17][CH2:18][CH2:19][CH2:20][CH:15]3[C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:43]=[CH:42][C:29]1=2)[CH3:41]

참가 물질

9

반응물 5

HCID 5238Sodium IodideHCID 11430Potassium CarbonateHCID 1030202-PhenylpiperidineHCID 21866389Hydrogen chloride-ethyl acetateHCID 686732537-(3-Chloropropoxy)-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione

생성물 1

HCID 669612001-Ethyl-3,3,5-trimethyl-7-[3-(2-phenylpiperidin-1-yl)propoxy]-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione hydrochloride수율 27.7%

시약·촉매·용매 3

HCID 962Water용매HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

반응 조건

온도
70 °C

실험 절차

Potassium carbonate(0.54 g), sodium iodide(0.21 g), and 2-phenyl piperidine(0.23 g) were added to a DMF solution(15 ml) of 7-(3-chloropropoxy)-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione(0.44 g). The mixture was stirred at 70° C. for 5 hours. The reaction mixture was cooled to room temperature. Water was added thereto, followed by extraction by ethyl acetate. The organic layer was washed with water and then with saturated saline, and dried with anhydrous magnesium sulfate. After condensation under reduced pressure, the residue was purified by silica gel column chromatography (hexane: ethyl acetate=2:1→1:1). The purified product was condensed under reduced pressure. A 4N-Hydrogen chloride ethyl acetate solution(0.2 ml) was added to an ethyl acetate solution (10 ml) of the residue, which was stirred at room temperature. The liquid was condensed to dryness under reduced pressure to give the title compound(0.18 g) as a white amorphous solid.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionfollowed by extraction by ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialwith saturated saline, and dried with anhydrous magnesium sulfate
  5. customAfter condensation under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (hexane: ethyl acetate=2:1→1:1)
  7. customcondensed under reduced pressure
  8. stirringwas stirred at room temperature
  9. customcondensed to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-579d65cebf9d4fabb686323271a804f2
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09212187B2

연결된 노트

불러오는 중…