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Aniline → N-cyano-N'-phenyl-4-pyridinecarboximidamide

HRID 327123
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HRID 327123 반응식
[C:1]([N:3]=[C:4]([C:9]1[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=1)OC(C)C)#[N:2].[NH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>CO>[C:1]([NH:3][C:4]([C:9]1[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=1)=[N:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)#[N:2]
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참가 물질

4

반응물 2

HCID 6115AnilineHCID 10012715Isopropyl N-cyano-4-pyridinecarboximidate

생성물 1

HCID 19734506N-cyano-N'-phenyl-4-pyridinecarboximidamide수율 54%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

Isopropyl N-cyano-4-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (5 ml), and aniline (0.27 g, 2.9 dissolved in methanol (5 ml) was added. The mixture was stirred at room temperature for 20 minutes. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 40 g). Elution with chloroform-methanol (100:1) gave the object compound, which was further crystallized from methanol-diethyl ether to give N-cyano-N'-phenyl-4-pyridinecarboximidamide (0.32 g, 1.4 mmol, yield: 54%) as colorless needles.

후처리

  1. additionwas added
  2. concentrationthe reaction solution was concentrated under reduced pressure
  3. concentrationThe residual concentrate
  4. washElution with chloroform-methanol (100:1)
  5. customgave the object compound, which
  6. customwas further crystallized from methanol-diethyl ether

출처 및 근거

ORD 기록
ord-51865948b1804aac867f4d9303284531
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05272164

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