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Chloroacetaldehyde → 2-fluoro-4-imidazo[1,2-a]pyrimidin-6-yl-N-methylbenzamide

HRID 1257787
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인쇄 미리보기

반응식

HRID 1257787 반응식
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([NH:14][CH3:15])=[O:13])=[C:10]([F:18])[CH:9]=2)=[CH:4][N:3]=1.Cl[CH2:20][CH:21]=O>C(O)(C)C>[F:18][C:10]1[CH:9]=[C:8]([C:5]2[CH:4]=[N:3][C:2]3[N:7]([CH:20]=[CH:21][N:1]=3)[CH:6]=2)[CH:17]=[CH:16][C:11]=1[C:12]([NH:14][CH3:15])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33ChloroacetaldehydeHCID 672245484-(2-aminopyrimidin-5-yl)-2-fluoro-N-methylbenzamide

생성물 1

HCID 672248512-fluoro-4-imidazo[1,2-a]pyrimidin-6-yl-N-methylbenzamide수율 88.8%

시약·촉매·용매 1

HCID 3776Isopropanol용매

반응 조건

온도
90 °C

실험 절차

A mixture of 4-(2-aminopyrimidin-5-yl)-2-fluoro-N-methylbenzamide (123 mg, 0.5 mmol) and chloroacetaldehyde (0.318 mL, 2.5 mmol) in isopropyl alcohol (4 mL) was stirred at 90° C. for 4 h. The solvent was removed under vacuum and the residue was triturated with ethyl acetate and hexanes. The solid formed was collected and dried under reduced pressure to give the desired product (120 mg, 88.8%). LCMS: (M+H)=271.0.

후처리

  1. customThe solvent was removed under vacuum
  2. customthe residue was triturated with ethyl acetate and hexanes
  3. customThe solid formed
  4. customwas collected
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-69a3636056ac4d6eaf170b9a8cfa885d
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461330B2

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