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Triethylamine → 1-[4-[(Methylsulfonyl)amino]benzoyl]aziridine

HRID 1199494
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HRID 1199494 반응식
[CH3:1][S:2]([NH:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](Cl)=[O:11])=[CH:8][CH:7]=1)(=[O:4])=[O:3].[NH:15]1[CH2:17][CH2:16]1.C(N(CC)CC)C>C(Cl)Cl>[CH3:1][S:2]([NH:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([N:15]2[CH2:17][CH2:16]2)=[O:11])=[CH:8][CH:7]=1)(=[O:4])=[O:3]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 9033AziridineHCID 117911194-[(Methylsulfonyl)amino]benzoyl chloride

생성물 1

HCID 147735491-[4-[(Methylsulfonyl)amino]benzoyl]aziridine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

13.0 g (55.6 mmol) of 4-[(methylsulfonyl)amino]benzoyl chloride is suspended in 150 mL of methylene chloride and cooled to about 0° C. 2.40 g (55.7 mmol) of aziridine and 7.75 mL (55.6 mmol) of triethylamine are added and the reaction allowed to warm to room temperature and stir for 2 hours. After 2 hours, the solution is washed with 100 mL of saturated aqueous sodium chloride and placed in the freezer. After 18 hours, the resulting white precipitate is filtered, washed with 50 mL of ether and dried to provide the title compound.

후처리

  1. temperatureto warm to room temperature
  2. waitAfter 2 hours
  3. washthe solution is washed with 100 mL of saturated aqueous sodium chloride
  4. waitAfter 18 hours
  5. filtrationthe resulting white precipitate is filtered
  6. washwashed with 50 mL of ether
  7. customdried

출처 및 근거

ORD 기록
ord-cab3e4b782604ee880c0f55346d0d0a3
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04900841

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