Methanol → 1-[5-[(Z)-2-cyano-2-(3,4-dimethoxy-phenyl)-vinyl]-thiophen-2-yl]-piperidin-4-yl[1,4']bipiperidinyl-1'-carboxylate hydrochloride

HRID 2366411ノート

反応式

HRID 2366411 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5](/[C:11](=[CH:14]/[C:15]2[S:16][C:17]([N:20]3[CH2:25][CH2:24][CH:23](O)[CH2:22][CH2:21]3)=[CH:18][CH:19]=2)/[C:12]#[N:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[Cl:27][C:28]([N:30]1[CH2:35][CH2:34][CH:33]([N:36]2[CH2:41][CH2:40][CH2:39][CH2:38][CH2:37]2)[CH2:32][CH2:31]1)=[O:29].C[OH:43]>N1C=CC=CC=1>[ClH:27].[C:12](/[C:11](/[C:5]1[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=1)=[CH:14]\[C:15]1[S:16][C:17]([N:20]2[CH2:25][CH2:24][CH:23]([CH:37]3[CH2:38][CH2:39][CH2:40][CH2:41][N:36]3[CH:33]3[CH2:34][CH2:35][N:30]([C:28]([OH:43])=[O:29])[CH2:31][CH2:32]3)[CH2:22][CH2:21]2)=[CH:18][CH:19]=1)#[N:13]

参加物

5

実験手順

Compound 6 (2.00 g) was dissolved in pyridine (50 mL), and 1-chlorocarbonyl-4-piperidinopiperidine (2.50 g) was added to the solution, followed by stirring under reflux for 2 hours. After completion of reaction, methanol was added to the reaction mixture, followed by stirring for 30 minutes. The solvent was evaporated under reduced pressure, and the residue was extracted with chloroform and purified water. The organic layer was dried over sodium sulfate anhydrate, and the solvent was evaporated to dryness. The residue was recrystallized from ethyl acetate, to thereby yield the target product (yield: 974 mg, 30%).

後処理

  1. temperatureunder reflux for 2 hours
  2. additionwas added to the reaction mixture
  3. stirringby stirring for 30 minutes
  4. customThe solvent was evaporated under reduced pressure
  5. extractionthe residue was extracted with chloroform
  6. custompurified water
  7. dry with materialThe organic layer was dried over sodium sulfate anhydrate
  8. customthe solvent was evaporated to dryness
  9. customThe residue was recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-496751a46a364fe58662320598d58b09
出典データセット
uspto-grants-2014_04
特許番号
US08697742B2

反応ノート

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