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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,8-Diazabicyclo(5.4.0)undec-7-ene → 1,2-Dihydro-1-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)-1,4,7b-triazacyclopent[cd]inden-2-one

HRID 1068775
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인쇄 미리보기

반응식

HRID 1068775 반응식
CS(O[CH2:6][CH:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]1)(=O)=O.[NH:20]1[C:28]2[N:23]3[C:24](=[N:29][CH:30]=[C:22]3[C:21]1=[O:31])[CH:25]=[CH:26][CH:27]=2.C1CCN2C(=NCCC2)CC1>CN(C=O)C.O>[C:16]([O:15][C:13]([N:10]1[CH2:11][CH2:12][CH:7]([CH2:6][N:20]2[C:28]3[N:23]4[C:24](=[N:29][CH:30]=[C:22]4[C:21]2=[O:31])[CH:25]=[CH:26][CH:27]=3)[CH2:8][CH2:9]1)=[O:14])([CH3:19])([CH3:18])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 2765838Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 117449051,2-Dihydro-1,4,7b-triazacyclopent[cd]inden-2-one

생성물 1

HCID 211901151,2-Dihydro-1-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)-1,4,7b-triazacyclopent[cd]inden-2-one수율 43.5%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6228Dimethylformamide용매

실험 절차

A mixture containing 5.68 g (20.0 mM) of (1-tert-butoxycarbonylpiperidin-4-ylmethyl) methanesulfonate, 4.35 g (20.0 mM) of 1,2-dihydro-1,4,7b-triazacyclopent[cd]inden-2-one.2NaCl, and 3.58 ml (24.0 mM) of DBU in 50 ml of DMF was heated at 80° C. for 2 hours. After completion of the reaction, the reaction mixture was poured in 50 ml of iced water and extracted with 100 ml of ethyl acetate. The organic layer was washed with 50 ml of purified water twice and, then, with 50 ml of saturated aqueous NaCl solution and dried over Na2SO4. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel column chromatography (eluent: ethyl acetate-ethanol=10:1) to provide 3.00 g (yield 42.1%) of the title compound as a brown amorphous substance.

후처리

  1. customAfter completion of the reaction
  2. extractionextracted with 100 ml of ethyl acetate
  3. washThe organic layer was washed with 50 ml of purified water twice
  4. dry with materialwith 50 ml of saturated aqueous NaCl solution and dried over Na2SO4
  5. distillationThe solvent was then distilled off under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (eluent: ethyl acetate-ethanol=10:1)

출처 및 근거

ORD 기록
ord-a64ba7d79c854b4fa94b4744f47d8359
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06251905B1

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