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3-Pyridinecarbonyl chloride, hydrochloride (1:1) → HCID 60205314, 화합물

HRID 408185
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HRID 408185 반응식
Cl.[C:2](Cl)(=[O:9])[C:3]1[CH:8]=[CH:7][CH:6]=[N:5][CH:4]=1.[F:11][C:12]1[C:17]([F:18])=[CH:16][N:15]=[C:14]2[NH:19][CH:20]=[C:21]([NH2:22])[C:13]=12>N1C=CC=CC=1>[F:11][C:12]1[C:17]([F:18])=[CH:16][N:15]=[C:14]2[NH:19][CH:20]=[C:21]([NH:22][C:2](=[O:9])[C:3]3[CH:8]=[CH:7][CH:6]=[N:5][CH:4]=3)[C:13]=12
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참가 물질

4

반응물 2

HCID 884383-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 60205313HCID 60205313, 화합물

생성물 1

HCID 60205314HCID 60205314, 화합물수율 92.6%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Nicotinoyl chloride hydrochloride (0.70 g, 3.90 mmol) was added to 4,5-difluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (0.22 g, 1.30 mmol) in pyridine (5 mL). The reaction was stirred at room temperature for 10 minutes, and then the pyridine was removed. THF (5 mL) and 2N LiOH (3 mL) were added, and the reaction was stirred for 20 minutes. The THF was removed, and water (20 mL) was added. The solid formed was collected by filtration and dried to give N-(4,5-difluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)nicotinamide (0.33 g, 92% yield) as a solid.

후처리

  1. customthe pyridine was removed
  2. additionTHF (5 mL) and 2N LiOH (3 mL) were added
  3. stirringthe reaction was stirred for 20 minutes
  4. customThe THF was removed
  5. additionwater (20 mL) was added
  6. customThe solid formed
  7. filtrationwas collected by filtration
  8. customdried

출처 및 근거

ORD 기록
ord-d564eb62598e4022b783ccbceed9f4f1
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08758830B2

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