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Cyclopropylamine → 2-(Cyclopropylamino)-N-(2-methoxy-4-methyl-3-pyridinyl)-3-pyridinecarboxamide

HRID 1734123
노트
인쇄 미리보기

반응식

HRID 1734123 반응식
Cl[C:2]1[C:7]([C:8]([NH:10][C:11]2[C:12]([O:18][CH3:19])=[N:13][CH:14]=[CH:15][C:16]=2[CH3:17])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH:20]1([NH2:23])[CH2:22][CH2:21]1>>[CH:20]1([NH:23][C:2]2[C:7]([C:8]([NH:10][C:11]3[C:12]([O:18][CH3:19])=[N:13][CH:14]=[CH:15][C:16]=3[CH3:17])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=2)[CH2:22][CH2:21]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 69828CyclopropylamineHCID 104236502-Chloro-N-(2-methoxy-4-methyl-3-pyridinyl)-3-pyridinecarboxamide

생성물 1

HCID 104474082-(Cyclopropylamino)-N-(2-methoxy-4-methyl-3-pyridinyl)-3-pyridinecarboxamide수율 86%

반응 조건

온도
110 °C

실험 절차

2-Chloro-N-(2-methoxy-4-methyl-3-pyridinyl)-3-pyridinecarboxamide (0.55 g, 2 mmol) was placed in a sealed tube containing cyclopropylamine (0.5 mL, 7 mmol) and heated to 110° C. overnight. Removal of the cyclopropylamine by rotary evaporation followed by flash chromatography of the residue on silica gel (1:1 EtOAc:hexanes) gave the desired compound in 86% yield (0.51 g). m.p.: 151°-152° C. (Recrystallized from heptane).

후처리

  1. customRemoval of the cyclopropylamine
  2. customby rotary evaporation

출처 및 근거

ORD 기록
ord-b74d61fbe4d743d8934a5c97d9ac0506
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05532358

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