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Isopropylamine → 2-n-Butyl-3-[4-(2-hydroxy-3-isopropylaminopropoxy)phenylsulfonyl]benzofuran

HRID 1764664
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인쇄 미리보기

반응식

HRID 1764664 반응식
[CH2:1]([C:5]1[O:6][C:7]2[CH:27]=[CH:26][CH:25]=[CH:24][C:8]=2[C:9]=1[S:10]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:20][CH:21]2[O:23][CH2:22]2)=[CH:15][CH:14]=1)(=[O:12])=[O:11])[CH2:2][CH2:3][CH3:4].[CH:28]([NH2:31])([CH3:30])[CH3:29]>C(Cl)(Cl)Cl>[CH2:1]([C:5]1[O:6][C:7]2[CH:27]=[CH:26][CH:25]=[CH:24][C:8]=2[C:9]=1[S:10]([C:13]1[CH:14]=[CH:15][C:16]([O:19][CH2:20][CH:21]([OH:23])[CH2:22][NH:31][CH:28]([CH3:30])[CH3:29])=[CH:17][CH:18]=1)(=[O:11])=[O:12])[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 227688372-n-Butyl-3-[4-(2,3-epoxypropoxy)phenylsulfonyl]benzofuran

생성물 1

HCID 227688812-n-Butyl-3-[4-(2-hydroxy-3-isopropylaminopropoxy)phenylsulfonyl]benzofuran

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2-n-Butyl-3-[4-(2,3-epoxypropoxy)phenylsulfonyl]benzofuran (1.9 g.) was dissolved in 30 ml. of freshly distilled isopropylamine and the solution was heated at 100° for 2 hours. After cooling, the solvent was evaporated to give a residue which was dissolved in chloroform. Evaporation of the solvent gave the title compound.

후처리

  1. temperatureAfter cooling
  2. customthe solvent was evaporated
  3. customto give a residue which
  4. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-46ca60b29d5c464db13c4d25eeee43c6
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04117128

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