홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 1162009
노트
인쇄 미리보기

반응식

HRID 1162009 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3301EthylenediamineHCID 12091293,4-Dichlorosulfolane, cis-

생성물 1

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

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

반응 조건

온도
100 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1d19620b5b0a4015bfdfd4e5ea4f7724
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820675B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트