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

Tetrahydrofuran → 3-{9-[8-(2,2,2-Trifluoro-acetyl)-8-aza-bicyclo[3.2.1]oct-3-ylidene]-9H-xanthen-3-yl}-4H-[1,2,4]thiadiazol-5-one

HRID 1987945
노트
인쇄 미리보기

반응식

HRID 1987945 반응식
O[NH:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]2[C:9](=[C:19]3[CH2:25][CH:24]4[N:26]([C:27](=[O:32])[C:28]([F:31])([F:30])[F:29])[CH:21]([CH2:22][CH2:23]4)[CH2:20]3)[C:10]3[C:15]([O:16][C:17]=2[CH:18]=1)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[NH:4].C1N=CN([C:38](N2C=NC=C2)=[S:39])C=1.C1C[O:48]CC1>O>[F:29][C:28]([F:31])([F:30])[C:27]([N:26]1[CH:24]2[CH2:23][CH2:22][CH:21]1[CH2:20][C:19](=[C:9]1[C:8]3[CH:7]=[CH:6][C:5]([C:3]4[NH:2][C:38](=[O:48])[S:39][N:4]=4)=[CH:18][C:17]=3[O:16][C:15]3[C:10]1=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH2:25]2)=[O:32]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 802641,1'-ThiocarbonyldiimidazoleHCID 178513222HCID 178513222, 화합물

생성물 1

HCID 1359999753-{9-[8-(2,2,2-Trifluoro-acetyl)-8-aza-bicyclo[3.2.1]oct-3-ylidene]-9H-xanthen-3-yl}-4H-[1,2,4]thiadiazol-5-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of compound 6a (0.0417 g, 0.094 mmol) and TCDI (0.025 g, 0.14 mmol) in THF (2 mL) was stirred at room temperature for 45 min. The mixture was diluted with H2O (2 mL) and extracted with EtOAc (3×5 mL). The combined organic extracts were washed with H2O (15 mL), dried (MgSO4), and concentrated. The residue was dissolved in THF (2 mL). Boron trifluoride diethyl etherate was added to the solution, and the resulting mixture was stirred at room temperature for 1 h. The mixture was diluted with H2O (2 mL) and extracted with EtOAc (3×5mL). The organic layers were dried (MgSO4), and concentrated. The resultant compound 9a was used in the next reaction without further purification. MS m/z (MH+) 485.8.

후처리

  1. extractionextracted with EtOAc (3×5 mL)
  2. washThe combined organic extracts were washed with H2O (15 mL)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in THF (2 mL)
  6. additionBoron trifluoride diethyl etherate was added to the solution
  7. stirringthe resulting mixture was stirred at room temperature for 1 h
  8. additionThe mixture was diluted with H2O (2 mL)
  9. extractionextracted with EtOAc (3×5mL)
  10. dry with materialThe organic layers were dried (MgSO4)
  11. concentrationconcentrated
  12. customThe resultant compound 9a was used in the next reaction without further purification

출처 및 근거

ORD 기록
ord-2567296273fa4e6985ddcf045f8e1231
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07553850B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트