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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonium Hydroxide → HCID 57562895, 화합물

HRID 1770818
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HRID 1770818 반응식
Cl[S:2]([C:5]1[CH:6]=[C:7]([N+:13]([O-:15])=[O:14])[CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])(=[O:4])=[O:3].[OH-].[NH4+:17]>C(OCC)(=O)C>[NH2:17][S:2]([C:5]1[CH:6]=[C:7]([N+:13]([O-:15])=[O:14])[CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])(=[O:4])=[O:3]
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참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 575628802-Fluoro-3-methyl-5-nitrobenzene-1-sulfonyl chloride

생성물 1

HCID 57562895HCID 57562895, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

The resulting oily residue of compound 26 was taken up in ethyl acetate (100 mL) and stirred with ammonium hydroxide (100 mL, 30% aqueous solution) overnight at room temperature. After the ethyl acetate layer was separated, the aqueous layer was extracted with ethyl acetate (2×50 mL). The organic layers were combined, dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The dark oily residue was chromatographed (silica gel, hexanes then 10%, 20%, up to 50% ethyl acetate in hexanes to afford 3-aminosulfonyl-4-fluoro-5-methylnitrobenzene (27). LCMS: purity: 89%; MS (m/z): 235 (MH+).

후처리

  1. customAfter the ethyl acetate layer was separated
  2. extractionthe aqueous layer was extracted with ethyl acetate (2×50 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. customthe solvent was removed under vacuum
  5. customThe dark oily residue was chromatographed (silica gel, hexanes

출처 및 근거

ORD 기록
ord-a947b3a8037b460fb90d9207dd6c8976
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09248190B2

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