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4-Fluoro-3-(morpholine-4-sulfonyl)benzoic acid → 4-Mercapto-3-(morpholine-4-sulfonyl)-benzoic Acid

HRID 277572
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HRID 277572 반응식
O.[SH-:2].[Na+].F[C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][C:6]=1[S:14]([N:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1)(=[O:16])=[O:15]>CN(C=O)C>[SH:2][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][C:6]=1[S:14]([N:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1)(=[O:16])=[O:15]
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참가 물질

4

반응물 2

HCID 6927164-Fluoro-3-(morpholine-4-sulfonyl)benzoic acidHCID 16211346Sodium hydrosulfide hydrate

생성물 1

HCID 226290394-Mercapto-3-(morpholine-4-sulfonyl)-benzoic Acid수율 89.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

Sodium hydrosulfide monohydrate (237 mg, 4.3 mmol) was added to a solution of 4-fluoro-3-(morpholine-4-sulfonyl)-benzoic acid (Example 6, 350 mg, 1.2 mmol) in DMF (15 mL) and the reaction mixture was heated at 60° C. for 20 hours under N2. After cooling to room temperature and quenching with 2M HCl, the reaction mixture was partitioned between ethyl acetate and water. Further extraction of the aqueous layer with ethyl acetate, combination of all organic layers, drying and concentration provided a white powder (326 mg, 89% yield): 1HNMR DMSO-d6) δ2.99 (t, J=4 Hz, 4H), 3.58 (t, J=4. Hz, H), 7.48 (d, J=8 Hz,1H), 7.87 (dd, J=8, 2 Hz, 1H), 8.29 (d, J=2 Hz, 1H), 13.20 (s, 1H): MS (ESI) [M−H]− m/z 304.

후처리

  1. temperatureAfter cooling to room temperature
  2. customquenching with 2M HCl
  3. customthe reaction mixture was partitioned between ethyl acetate and water
  4. extractionFurther extraction of the aqueous layer with ethyl acetate, combination of all organic layers
  5. customdrying
  6. concentrationconcentration

출처 및 근거

ORD 기록
ord-e294ca167e124d8e8f95b243a2f7dcb4
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06355633B1

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