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Sodium Chloride → 4-Methoxyphenyl-1-[5-isopropyl-2,4-bis(methoxymethoxy)-benzoyl]thiosemicarbazide

HRID 1947184
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HRID 1947184 반응식
[CH:1]([C:4]1[C:5]([O:17][CH2:18][O:19][CH3:20])=[CH:6][C:7]([O:13][CH2:14][O:15][CH3:16])=[C:8]([CH:12]=1)[C:9]([OH:11])=O)([CH3:3])[CH3:2].[CH3:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([NH:29][NH:30][C:31]([NH2:33])=[S:32])=[CH:25][CH:24]=1.O.ON1C2C=CC=CC=2N=N1.CN(C)CCCN=C=NCC.[Cl-].[Na+]>CN(C)C=O>[CH3:21][O:22][C:23]1[CH:24]=[CH:25][C:26]([N:29]([C:9](=[O:11])[C:8]2[CH:12]=[C:4]([CH:1]([CH3:2])[CH3:3])[C:5]([O:17][CH2:18][O:19][CH3:20])=[CH:6][C:7]=2[O:13][CH2:14][O:15][CH3:16])[NH:30][C:31]([NH2:33])=[S:32])=[CH:27][CH:28]=1
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참가 물질

7

반응물 5

HCID 5234Sodium ChlorideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 27960291-Hydroxybenzotriazole hydrateHCID 28261724-MethoxyphenylthiosemicarbazideHCID 58236465HCID 58236465, 화합물

생성물 1

HCID 866243104-Methoxyphenyl-1-[5-isopropyl-2,4-bis(methoxymethoxy)-benzoyl]thiosemicarbazide
수율 86.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

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온도
0 °C

실험 절차

5-isopropyl-2,4-bis(methoxymethoxy)-benzoic acid (IM3-a: 16.4 g, 54.5 mmol), 4-methoxyphenylthiosemicarbazide (F53-02: 11.3 g, 57.3 mmol), dimethylformamide (150 mL) and 1-hydroxybenzotriazole monohydrate (8.11 g, 60.0 mmol) were placed in a 500 mL eggplant shaped flask. The reaction mixture was cooled to 0° C. and mixed with a suspension of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (11.5 g, 60 mmol) in dimethylformamide (100 mL). The mixture was stirred for 4 hours and allowed to come to room temperature. After completing the reaction, saturated sodium chloride solution (500 mL) was added to the reaction mixture, and the mixture was extracted twice with ethyl acetate (500 mL). The organic layer thus obtained was washed 4 times with saturated sodium chloride solution (500 mL) and dried over anhydrous sodium sulfate. After removing sodium sulfate by filtration, the solvent was distilled under reduced pressure, and the solids obtained were suspended in hexane (1000 mL) for purification and collected by filtration. The solids thus obtained were dried under reduced pressure to obtain the title compound (F53-03: 21.9 g, 83.8%).

후처리

  1. customto come to room temperature
  2. additionwas added to the reaction mixture
  3. extractionthe mixture was extracted twice with ethyl acetate (500 mL)
  4. customThe organic layer thus obtained
  5. washwas washed 4 times with saturated sodium chloride solution (500 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customAfter removing sodium sulfate
  8. filtrationby filtration
  9. distillationthe solvent was distilled under reduced pressure
  10. customthe solids obtained
  11. customwere suspended in hexane (1000 mL) for purification
  12. filtrationcollected by filtration
  13. customThe solids thus obtained
  14. customwere dried under reduced pressure

출처 및 근거

ORD 기록
ord-3160f81211b746b295615af0cac7dbfb
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399464B2

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