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Isopropylamine → 1-(2-Cyano-4-n-hexanoylamino-phenoxy)-3-isopropylamino-2-propanol

HRID 1903748
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HRID 1903748 반응식
[C:1]([C:3]1[CH:13]=[C:12]([NH:14][C:15](=[O:21])[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:11]=[CH:10][C:4]=1[O:5][CH2:6][CH:7]1[O:9][CH2:8]1)#[N:2].[CH:22]([NH2:25])([CH3:24])[CH3:23]>C(O)C>[C:1]([C:3]1[CH:13]=[C:12]([NH:14][C:15](=[O:21])[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:11]=[CH:10][C:4]=1[O:5][CH2:6][CH:7]([OH:9])[CH2:8][NH:25][CH:22]([CH3:24])[CH3:23])#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 12939818HCID 12939818, 화합물

생성물 1

HCID 127640311-(2-Cyano-4-n-hexanoylamino-phenoxy)-3-isopropylamino-2-propanol

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ten grams (0.035 mol) of 1-(2-cyano-4-hexanoylamino-phenoxy)-2,3-epoxypropane were dissolved in 100 ml of ethanol and, after the addition of 8.3 gm (0.14 mol) of isopropylamine, the mixture was refluxed for one hour. The solvent was evaporated in vacuo, and the remaining residue solidified. It was recrystallized twice from acetonitrile. The white crystalline base was recovered by suction filtration and dried.

후처리

  1. temperaturethe mixture was refluxed for one hour
  2. customThe solvent was evaporated in vacuo
  3. customIt was recrystallized twice from acetonitrile
  4. filtrationThe white crystalline base was recovered by suction filtration
  5. customdried

출처 및 근거

ORD 기록
ord-07f3f5c02e1d4158a7a42e09fbd3d9e5
출처 데이터셋
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04438143

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