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Benzylamine → 2-Benzylamino-4-amino-5-fluoropyridine

HRID 368460
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HRID 368460 반응식
CN1CCCC1=O.[NH2:8][C:9]1[C:14]([F:15])=[CH:13][N:12]=[C:11](F)[CH:10]=1.[CH2:17]([NH2:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C(Cl)(Cl)Cl>[CH2:17]([NH:24][C:11]1[CH:10]=[C:9]([NH2:8])[C:14]([F:15])=[CH:13][N:12]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7504BenzylamineHCID 13387N-methyl-2-pyrrolidoneHCID 221211752,5-Difluoropyridin-4-amine

생성물 1

HCID 221212872-Benzylamino-4-amino-5-fluoropyridine수율 58.4%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To 1 ml of N-methylpyrrolidone was added 410 mg of 4-amino-2,5-difluoropyridine together with 930 mg of benzylamine, and the mixture was allowed to react in nitrogen atmosphere at 150° C. for 3 days and allowed to cool. After adding 30 ml of chloroform, the mixture was washed twice with 300 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography (silica gel, 15 g; eluent: chloroform:methanol, 1:0 and then, 50:1) to obtain 400 mg of the title compound as a colorless solid.

후처리

  1. customto react in nitrogen atmosphere at 150° C. for 3 days
  2. temperatureto cool
  3. washthe mixture was washed twice with 300 ml of distilled water
  4. dry with materialThe chloroform layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e81e8d39d9f849a5ab6e1206f0f5689b
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06133284

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