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Dimethylformamide → HCID 68193064、化合物

HRID 2193149
ノート
印刷プレビュー

反応式

HRID 2193149 の反応式
CN(C)C=O.[C:6]([O:10][C:11](=[O:46])[N:12]([CH:24]1[CH2:29][CH2:28][N:27]([CH2:30][CH2:31][N:32]2[C:41]3[C:36](=[C:37](Br)[CH:38]=[C:39]([O:42][CH3:43])[CH:40]=3)[CH:35]=[CH:34][C:33]2=[O:45])[CH2:26][CH2:25]1)[CH2:13][C:14]1[CH:23]=[CH:22][C:17]2[O:18][CH2:19][CH2:20][O:21][C:16]=2[CH:15]=1)([CH3:9])([CH3:8])[CH3:7].[C:47]([O:51][CH2:52][CH3:53])(=[O:50])[CH:48]=[CH2:49]>CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C.C(N(CC)CC)C>[C:6]([O:10][C:11]([N:12]([CH2:13][C:14]1[CH:23]=[CH:22][C:17]2[O:18][CH2:19][CH2:20][O:21][C:16]=2[CH:15]=1)[CH:24]1[CH2:29][CH2:28][N:27]([CH2:30][CH2:31][N:32]2[C:41]3[C:36](=[C:37](/[CH:49]=[CH:48]/[C:47]([O:51][CH2:52][CH3:53])=[O:50])[CH:38]=[C:39]([O:42][CH3:43])[CH:40]=3)[CH:35]=[CH:34][C:33]2=[O:45])[CH2:26][CH2:25]1)=[O:46])([CH3:9])([CH3:8])[CH3:7]
参加物反応条件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 6228DimethylformamideHCID 8821Ethyl AcrylateHCID 59397948tert-butyl (1-(2-(5-bromo-7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)carbamate

生成物 1

HCID 68193064HCID 68193064、化合物

試薬・触媒・溶媒 2

HCID 178418851HCID 178418851、化合物触媒
HCID 8471
Triethylamine
溶媒

反応条件

温度
90 °C

実験手順

To 4.0 mL of an N,N-dimethylformamide solution containing 0.15 g of tert-butyl(1-(2-(5-bromo-7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)carbamate, 39 μl of ethyl acrylate, 50 μL of triethylamine and 6.1 mg of bis(tri-tert-butylphosphine)palladium(0) were added and heated under nitrogen atmosphere at 90° C. for 1.5 hours. The reaction mixture was cooled to the room temperature, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=20:1] to give 0.15 g of ethyl (2E)-3-(1-(2-(4-((tert-butoxycarbonyl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-5-yl)acrylate as a light brown foam.

後処理

  1. additionwere added
  2. temperatureThe reaction mixture was cooled to the room temperature
  3. customthe solvent was removed under reduced pressure
  4. customThe residue thus obtained
  5. customwas purified by silica gel column chromatography [eluent; chloroform:methanol=20:1]

出典と根拠

ORDレコード
ord-4cc208af5e2d4523995400b326991e89
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329694B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート