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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
ノート
印刷プレビュー

反応式

HRID 1068775 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-a64ba7d79c854b4fa94b4744f47d8359
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06251905B1

反応ノート

読み込み中…

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