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Tetrahydrofuran → HCID 14579134, 화합물

HRID 2248358
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HRID 2248358 반응식
[CH2:1]1[CH2:5][O:4][CH2:3][CH2:2]1.[O:6]1C=[CH:9][CH:8]=[C:7]1[NH:11][CH2:12][C:13]#[N:14].[CH3:15][N:16]1[CH:20]=C(C(Cl)=O)C=[N:17]1>C(N(CC)CC)C>[C:13]([CH:12]([C:3]1[O:4][CH:5]=[CH:1][CH:2]=1)[NH:11][C:7]([C:8]1[CH:9]=[N:17][N:16]([CH3:20])[CH:15]=1)=[O:6])#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 31649311-methyl-1H-pyrazole-4-carbonyl chlorideHCID 19996059HCID 19996059, 화합물

생성물 1

HCID 14579134HCID 14579134, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

To a THF solution containing the α-(2-furyl)aminoacetonitrile (2.15 g) and triethylamine (1.75 g) was added 1-methyl-1H-pyrazole-4-carboxylic acid chloride (2.55 g) under cooling with ice, and the whole was stirred for 1 hour as such and then for 16 hours at room temperature. The solid product formed was taken out by filtration, and the solvent was evaporated out, and then the thus-obtained oily product was purified by column chromatography and then washed with isopropyl ether, to give 2.55 g of the intended N-(cyano-2-furanylmethyl)-1-methyl-1H-pyrazole-4-carboxamide crystal.

후처리

  1. temperatureunder cooling with ice
  2. customThe solid product formed
  3. filtrationwas taken out by filtration
  4. customthe solvent was evaporated out
  5. customthe thus-obtained oily product was purified by column chromatography
  6. washwashed with isopropyl ether

출처 및 근거

ORD 기록
ord-5db9dbf3bf37400492e3d6f96a4f0ff1
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05039694

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