Chlorosuccinimide → 4-[2-(Dipropylamino)ethyl]indol-2-one

HRID 1766628노트

반응식

HRID 1766628 반응식
Cl[N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=O.[CH2:9]([N:12]([CH2:24][CH2:25][CH3:26])[CH2:13][CH2:14][C:15]1C=CC=C2[C:16]=1[CH:17]=[CH:18]N2)[CH2:10][CH3:11]>C1(C)C=CC=CC=1>[CH2:24]([N:12]([CH2:9][CH2:10][CH3:11])[CH2:13][CH2:14][C:15]1[C:4]2[C:3]([CH:18]=[CH:17][CH:16]=1)=[N:2][C:6](=[O:7])[CH:5]=2)[CH2:25][CH3:26]

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 30860544-(2-di-N-propylaminoethyl)indole

생성물 1

HCID 211117034-[2-(Dipropylamino)ethyl]indol-2-one수율 66.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

N-chlorosuccinimide (2.52 g, 18.9 mmol) was added to a solution of 4-[2-(dipropylamino)ethyl]indole (IV) (3 g, 12.28 mmol) in toluene (10 mL) and was stirred at room temperature for 1 h. The resultant mixture was washed with an aqueous solution of NaOH 5% and then an aqueous solution of HCl 1N (30 mL) was added to the organic layer and was heated at reflux temperature for 1 h. When the mixture reached room temperature, the organic layer was separated and the aqueous layer was basified with an aqueous solution of NaOH and extracted with AcOEt. The organic layer was dried, filtered and concentrated to obtain 2.1 g (66%) of 4-[2-(dipropylamino)ethyl]indol-2-one (I), which was purified and converted into its hydrochloride salt.

후처리

  1. washThe resultant mixture was washed with an aqueous solution of NaOH 5%
  2. additionan aqueous solution of HCl 1N (30 mL) was added to the organic layer
  3. temperaturewas heated
  4. temperatureat reflux temperature for 1 h
  5. customreached room temperature
  6. customthe organic layer was separated
  7. extractionextracted with AcOEt
  8. customThe organic layer was dried
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-75d8e5b705d24ac4b7b7cf1e1bafe3a8
출처 데이터셋
uspto-grants-2007_06
특허 번호
US07230118B2

반응 노트

불러오는 중…