4-Methylmorpholine → HCID 59140422, 화합물

HRID 425317노트

반응식

HRID 425317 반응식
CN1CCOCC1.[CH3:8][C:9]([CH3:18])([CH2:16][CH3:17])[CH2:10][C:11]1[N:12]=[CH:13][NH:14][CH:15]=1.[CH3:19][N:20]([CH3:25])[S:21](Cl)(=[O:23])=[O:22]>C(COC)OC>[CH3:8][C:9]([CH3:18])([CH2:16][CH3:17])[CH2:10][C:11]1[N:12]=[CH:13][N:14]([S:21]([N:20]([CH3:25])[CH3:19])(=[O:23])=[O:22])[CH:15]=1

참가 물질

5

반응물 3

HCID 79724-Methylmorpholine2회HCID 83372Dimethylsulphamoyl chloride2회HCID 178442466HCID 178442466, 화합물

생성물 1

HCID 59140422HCID 59140422, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

반응 조건

온도
40 °C

실험 절차

N-methylmorpholine (54 mL, 0.48 mol) was added to a solution of 4-(2,2-dimethylbutyl)-1H-imidazole (36 g, 0.24 mol) in dimethoxyethane (360 mL). After warming to 40° C., N,N-dimethylsulfamoyl chloride (38 mL, 0.36 mol) was added over 15 min. After stirring at 40° C. for 2 h, N-methylmorpholine (11 mL) and N,N-dimethylsulfamoyl chloride (8 mL) were added. After stirring for an additional 2 h the reaction mixture was cooled and filtered rinsing with ether. The filtrate was extracted with ether. The combined organic extracts were washed with brine, dried (magnesium sulfate), filtered, concentrated in vacuo. Chromatography over silica afforded the title compound.

후처리

  1. stirringAfter stirring for an additional 2 h the reaction mixture
  2. temperaturewas cooled
  3. filtrationfiltered
  4. washrinsing with ether
  5. extractionThe filtrate was extracted with ether
  6. washThe combined organic extracts were washed with brine
  7. dry with materialdried (magnesium sulfate)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-91aa6d17c34f4f47a6bce784cf33d0cb
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08106070B2

반응 노트

불러오는 중…