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1-(Methylsulfanyl)propan-2-amine → 4-(2-chloro-4-pyridinyl)-N-[1-methyl-2-(methylthio)ethyl]-2-pyrimidinamine

HRID 913289
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인쇄 미리보기

반응식

HRID 913289 반응식
Cl[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([Cl:14])[CH:9]=2)[CH:5]=[CH:4][N:3]=1.[CH3:15][S:16][CH2:17][CH:18]([NH2:20])[CH3:19]>C1(C)C=CC=CC=1>[Cl:14][C:10]1[CH:9]=[C:8]([C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:20][CH:18]([CH3:19])[CH2:17][S:16][CH3:15])[N:7]=2)[CH:13]=[CH:12][N:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120973921-(Methylsulfanyl)propan-2-amine2회HCID 581026912-Chloro-4-(2-chloropyridin-4-yl)pyrimidine

생성물 1

HCID 866467764-(2-chloro-4-pyridinyl)-N-[1-methyl-2-(methylthio)ethyl]-2-pyrimidinamine수율 88%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
60 °C

실험 절차

To a solution of 2-chloro-4-(2-chloro-4-pyridinyl)pyrimidine (i.e., the product of Example 6, Step A) (350 mg, 1.5 mmol) in toluene (4.0 mL) was added 1-(methylthio)-2-propanamine (i.e., the product of Step B) (1 mL, 9.5 mmol) in one portion; this mixture was heated at 60° C. for 18 h. The mixture was allowed to cool and silica gel (300 mg) was added. The excess solvent was removed under reduced pressure, and the resulting solid was chromatographed on silica gel eluted with a solvent gradient of 5% to 60% ethyl acetate in hexanes to give 400 mg (88%) of the title compound as a tan solid, m.p. 103-106° C.

후처리

  1. temperatureto cool
  2. additionsilica gel (300 mg) was added
  3. customThe excess solvent was removed under reduced pressure
  4. customthe resulting solid was chromatographed on silica gel
  5. washeluted with a solvent gradient of 5% to 60% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-9d74fb1551304cd48b20909b6be9434c
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08026359B2

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