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Ethylenediamine → Octahydrothieno[3,4-b]pyrazine 6,6-dioxide

HRID 1162009
ノート
印刷プレビュー

反応式

HRID 1162009 の反応式
Cl[C@H:2]1[C@@H:6](Cl)[CH2:5][S:4](=[O:9])(=[O:8])[CH2:3]1.[CH2:10]([NH2:13])[CH2:11][NH2:12]>O1CCOCC1>[NH:12]1[CH2:11][CH2:10][NH:13][CH:2]2[CH2:3][S:4](=[O:9])(=[O:8])[CH2:5][CH:6]12
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 3301EthylenediamineHCID 12091293,4-Dichlorosulfolane, cis-

生成物 1

HCID 16449569Octahydrothieno[3,4-b]pyrazine 6,6-dioxide収率 59%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
100 °C

実験手順

cis-3,4-Dichlorotetrahydrothiophene 1,1-dioxide (5.0 g, 26.0 mmol) in dioxane (40 mL) was added dropwise to ethane-1,2-diamine (10.4 g, 173.0 mmol) in dioxane (25 mL) at 0° C. The mixture was heated at 100° C. for 3 h, followed by cooling to room temperature and continued stirring overnight. The two layers were separated and the bottom layer, containing ethylene diamine and amine salt, was washed twice with dioxane. The dioxane layers were combined and the solvent was removed in vacuo. The crude product was recrystallized from toluene to afford 2.7 g (59%) of the title compound as white crystals. HPLC 98%, RT: 0.292 (System B; 10-97% MeCN over 3 min). 1H NMR (270 MHz, methanol-d4) δ ppm 2.67-2.76 (m, 2H) 2.86-2.96 (m, 2H) 3.13-3.20 (m, 2H) 3.33-3.44 (m, 2H) 3.63-3.70 (m, 2H). LC-MS 177 (M+H)+. *Previously described in U.S. Pat. No. 3,882,122.

後処理

  1. temperatureby cooling to room temperature
  2. customThe two layers were separated
  3. additionthe bottom layer, containing ethylene diamine and amine salt
  4. washwas washed twice with dioxane
  5. customthe solvent was removed in vacuo
  6. customThe crude product was recrystallized from toluene

出典と根拠

ORDレコード
ord-1d19620b5b0a4015bfdfd4e5ea4f7724
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07820675B2

反応ノート

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