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

HRID 1596727
ノート
印刷プレビュー

反応式

HRID 1596727 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8150Diglyme溶媒

反応条件

温度
160 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-d5fd7940dd4c4e9a9ee6ccfa74240cb9
出典データセット
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06291448B1

反応ノート

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