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Sulfamide → 1-Methyl-1,3-dihydro-2-thia-1,3-diaza-cyclopenta[B]naphthalene 2,2-dioxide

HRID 1596727
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HRID 1596727 반응식
[NH2:1][C:2]1[C:11]([NH:12][CH3:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[S:14](N)(N)(=[O:16])=[O:15]>COCCOCCOC>[CH3:13][N:12]1[C:11]2=[CH:10][C:9]3[C:4]([CH:3]=[C:2]2[NH:1][S:14]1(=[O:16])=[O:15])=[CH:5][CH:6]=[CH:7][CH:8]=3
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참가 물질

4

반응물 2

HCID 82267SulfamideHCID 217012522-Amino-3-methylamino-naphthalene

생성물 1

HCID 155380521-Methyl-1,3-dihydro-2-thia-1,3-diaza-cyclopenta[B]naphthalene 2,2-dioxide수율 69.7%

시약·촉매·용매 1

HCID 8150Diglyme용매

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온도
160 °C

실험 절차

A solution of 2-amino-3-methylamino-naphthalene (168 mg, 0.98 mmol) and sulfamide (44 mg, 0.98 mmol) in anhydrous diglyme (2 mL) was added dropwise over 5 minutes to a flask heated in a 160° C. oil bath. The reaction mixture was heated at 160° C. for an additional 30 minutes, then cooled to room temperature and evaporated under vacuum. The residue was partitioned between ethyl acetate (20 mL) and 2N hydrochloric acid (10 mL). The organic phase was washed with 2N hydrochloric acid (10 mL) and brine (10 mL), dried over magnesium sulfate, and evaporated under vacuum to afford the title compound (160 mg) as a solid.

후처리

  1. temperatureThe reaction mixture was heated at 160° C. for an additional 30 minutes
  2. temperaturecooled to room temperature
  3. customevaporated under vacuum
  4. customThe residue was partitioned between ethyl acetate (20 mL) and 2N hydrochloric acid (10 mL)
  5. washThe organic phase was washed with 2N hydrochloric acid (10 mL) and brine (10 mL)
  6. dry with materialdried over magnesium sulfate
  7. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-d5fd7940dd4c4e9a9ee6ccfa74240cb9
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06291448B1

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