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Isopropylamine → 4-Chloro-2-ethylamino-6-isopropylamino-5-pyrimidinecarbonitrile

HRID 372645
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반응식

HRID 372645 반응식
Cl[C:2]1[C:7]([C:8]#[N:9])=[C:6]([Cl:10])[N:5]=[C:4]([NH:11][CH2:12][CH3:13])[N:3]=1.[CH:14]([NH2:17])([CH3:16])[CH3:15]>CC(C)=O>[Cl:10][C:6]1[C:7]([C:8]#[N:9])=[C:2]([NH:17][CH:14]([CH3:16])[CH3:15])[N:3]=[C:4]([NH:11][CH2:12][CH3:13])[N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 205102564,6-Dichloro-2-ethylamino-5-pyrimidinecarbonitrile

생성물 1

HCID 205102214-Chloro-2-ethylamino-6-isopropylamino-5-pyrimidinecarbonitrile수율 94.7%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

To a stirred solution of 6.5 grams of 4,6-dichloro-2-ethylamino-5-pyrimidinecarbonitrile in 100 ml of acetone was added dropwise 7.4 grams of isopropylamine in 30 ml of acetone. Upon complete addition, the reaction mixture was stirred at room temperature for 16 hours. The acetone was removed by evaporation under reduced pressure, and the solid residue was washed with water. The resultant solid was collected by filtration to give 6.8 grams of 4-chloro-2-ethylamino-6-isopropylamino-5-pyrimidinecarbonitrile; mp 160°-165°. Recrystallization from a mixture of benzene and methylcyclohexane gave purified product; mp, 163°-165°.

후처리

  1. additionUpon complete addition
  2. customThe acetone was removed by evaporation under reduced pressure
  3. washthe solid residue was washed with water
  4. filtrationThe resultant solid was collected by filtration

출처 및 근거

ORD 기록
ord-fc23c464532649029808b723802f6192
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04092150

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