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

HCID 22405287, 화합물 → 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one

HRID 441222
노트
인쇄 미리보기

반응식

HRID 441222 반응식
C([O:3][C:4]([CH2:6][CH2:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:10]=1[N+:16]([O-])=O)=O)C>CO.C(O)(=O)C.[Fe]>[CH3:15][C:12]1[CH:13]=[CH:14][C:9]2[NH:8][CH2:7][CH2:6][C:4](=[O:3])[NH:16][C:10]=2[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 22405287HCID 22405287, 화합물

생성물 1

HCID 224052058-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one수율 16%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 176Acetic Acid용매HCID 887Methanol용매

실험 절차

A mixture of N-(2-ethoxycarbonylethyl)-4-methyl-2-nitroaniline (11.25 g) and iron powder (12.45 g) in a mixture of methanol (70 ml) and acetic acid (7 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was filtered through celite and the filtrate was evaporated in vacuo. The residue was dissolved with chloroform (50 ml) and the solution was basified with saturated sodium bicarbonate aqueous solution. The solution was filtered through celite and the organic layer was washed with brine. The solution was dried over magnesium sulfate and the solvent was removed. A mixture of the residue (8.00 g) in a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml) was refluxed for 1 hour and the solution was cooled to ambient temperature. The mixture was basified with concentrated ammonium hydroxide and then the resulting solution was extracted with chloroform. Drying over magnesium sulfate, filtering and the removal of solvents afforded a crude product. The crude product was triturated with diethyl ether - isopropyl ether (1:1) to give 8-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one (1.26 g) as a brown powder.

후처리

  1. temperaturewas refluxed for 1 hour
  2. filtrationThe mixture was filtered through celite
  3. customthe filtrate was evaporated in vacuo
  4. dissolutionThe residue was dissolved with chloroform (50 ml)
  5. filtrationThe solution was filtered through celite
  6. washthe organic layer was washed with brine
  7. dry with materialThe solution was dried over magnesium sulfate
  8. customthe solvent was removed
  9. additionA mixture of the residue (8.00 g)
  10. additionin a mixture of concentrated hydrochloric acid (16 ml) and water (12 ml)
  11. temperaturewas refluxed for 1 hour
  12. temperaturethe solution was cooled to ambient temperature
  13. extractionthe resulting solution was extracted with chloroform
  14. dry with materialDrying over magnesium sulfate
  15. filtrationfiltering
  16. customthe removal of solvents
  17. customafforded a crude product
  18. customThe crude product was triturated with diethyl ether - isopropyl ether (1:1)

출처 및 근거

ORD 기록
ord-879d11ac84554005b8862850a9437b3b
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05521170

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트