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Sodium Hydroxide → 4-Amino-2-fluoro-N-methylbenzenesulfonamide

HRID 407288
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HRID 407288 반응식
[F:1][C:2]1[CH:3]=[C:4]([NH:13]C(=O)C)[CH:5]=[CH:6][C:7]=1[S:8](=[O:12])(=[O:11])[NH:9][CH3:10].[OH-].[Na+]>Cl>[NH2:13][C:4]1[CH:5]=[CH:6][C:7]([S:8]([NH:9][CH3:10])(=[O:12])=[O:11])=[C:2]([F:1])[CH:3]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 34029456N-(3-fluoro-4-methylsulfamoylphenyl)acetamide

생성물 1

HCID 617181244-Amino-2-fluoro-N-methylbenzenesulfonamide수율 83.2%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

The above prepared N-(3-fluoro-4-methylsulfamoylphenyl)acetamide (1.55 g, 6.3 mmol) was suspended in 40 mL of 6M HCl and heated to reflux for 1 hr. The reaction was cooled in an ice bath and an NaOH solution was added to adjust the mixture to pH 5. The resulting white precipitate was isolated by filtration and was washed with water and dried to yield 1.07 g (83%) of the title compound. MS (m/z, ES+): 205.0 (M+1, 100%); 1H NMR (500 MHz, ppm, DMSO-d6): 7.35 (m, 1H), 7.12 (m, 1H), 6.40 (m, 2H), 6.23 (s, 2H), 2.40 (s, 3H).

후처리

  1. temperatureheated
  2. temperatureto reflux for 1 hr
  3. temperatureThe reaction was cooled in an ice bath
  4. customThe resulting white precipitate was isolated by filtration
  5. washwas washed with water
  6. customdried

출처 및 근거

ORD 기록
ord-e3551638fe274842ba9044c426687f27
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754233B2

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