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Isopropylamine → HCID 21287238, 화합물

HRID 868570
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HRID 868570 반응식
Br[CH2:2][CH2:3][N:4]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:7](=[O:8])[C:5]1=[O:6].[CH:15]([NH2:18])([CH3:17])[CH3:16]>CN(C)C=O>[CH:15]([NH:18][CH2:2][CH2:3][N:4]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:7](=[O:8])[C:5]1=[O:6])([CH3:17])[CH3:16]
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참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 35427341-(2-bromoethyl)-1H-indole-2,3-dione

생성물 1

HCID 21287238HCID 21287238, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 4.00 g of 1-(2-bromoethyl)isatin and 13.5 ml of isopropylamine in 160 ml of dry N,N-dimethylformamide was stirred for 1 hour at 80° C. The solution was concentrated under reduced pressure and the residue was dissolved in 50 ml of a 2N-hydrochloric acid. The solution was washed with ethyl acetate, neutralized by adding an aqueous sodium bicarbonate solution, and extracted with chloroform. The chloroform layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (eluent: chloroform/methanol=10/1) to obtain 3.11 g of 1-(2-isopropylaminoethyl)isatin in an oil.

후처리

  1. concentrationThe solution was concentrated under reduced pressure
  2. dissolutionthe residue was dissolved in 50 ml of a 2N-hydrochloric acid
  3. washThe solution was washed with ethyl acetate
  4. additionby adding an aqueous sodium bicarbonate solution
  5. extractionextracted with chloroform
  6. washThe chloroform layer was washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified with silica gel column chromatography (eluent: chloroform/methanol=10/1)

출처 및 근거

ORD 기록
ord-14d0d713f2664e72ac607c1a65fda7ca
출처 데이터셋
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04780477

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