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Benzoyl chloride → N-Methyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide

HRID 236894
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HRID 236894 반응식
[CH3:1][NH:2][C:3]1[S:4][C:5]([CH3:8])=[N:6][N:7]=1.[C:9](Cl)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>N1C=CC=CC=1>[CH3:1][N:2]([C:3]1[S:4][C:5]([CH3:8])=[N:6][N:7]=1)[C:9](=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7412Benzoyl chlorideHCID 3161286N,5-dimethyl-1,3,4-thiadiazol-2-amine

생성물 1

HCID 12679001N-Methyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2-(N-Methyl-amino)-5-methyl-1,3,4-thiadiazole (6 g, 0.046 mole) in pyridine (190 ml) was refluxed for 6 hours with benzoyl chloride (9.7 g, 0.069 mole) and the pyridine then evaporated off under reduced pressure. The residue was treated with water, made alkaline with sodium hydroxide solution and extracted with chloroform. The chloroform was washed with a saturated solution of sodium bicarbonate and a saturated solution of sodium chloride, dried, filtered and evaporated to yield title product which was recrystallised from ethanol.

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후처리

  1. customthe pyridine then evaporated off under reduced pressure
  2. additionThe residue was treated with water
  3. extractionextracted with chloroform
  4. washThe chloroform was washed with a saturated solution of sodium bicarbonate
  5. dry with materiala saturated solution of sodium chloride, dried
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-0f7d663c8805411e8a49469943e8724a
출처 데이터셋
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04158659

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