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Dimethyl Sulfoxide → 1-(2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-(3-pyridyl)piperidin-4-ol

HRID 1721760
ノート
印刷プレビュー

反応式

HRID 1721760 の反応式
[C:1](Cl)(=O)[C:2](Cl)=O.CS(C)=O.[Cl:11][C:12]1[CH:25]=[CH:24][C:23]2[CH:22]3[CH2:26][C:15]([CH2:27][N:28]4[CH2:33][CH2:32][CH:31]([OH:34])[CH2:30][CH2:29]4)([C:16]4[C:21]3=[CH:20][CH:19]=[CH:18][CH:17]=4)[C:14]=2[CH:13]=1.[CH2:35]([N:37](CC)[CH2:38]C)[CH3:36]>C(Cl)Cl>[Cl:11][C:12]1[CH:25]=[CH:24][C:23]2[CH:22]3[CH2:26][C:15]([CH2:27][N:28]4[CH2:29][CH2:30][C:31]([C:36]5[CH:35]=[N:37][CH:38]=[CH:1][CH:2]=5)([OH:34])[CH2:32][CH2:33]4)([C:16]4[C:21]3=[CH:20][CH:19]=[CH:18][CH:17]=4)[C:14]=2[CH:13]=1
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 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 214806821-(2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)piperidin-4-ol

生成物 1

HCID 214805851-(2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-(3-pyridyl)piperidin-4-ol収率 93%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
2 回

反応条件

温度
-78 °C

実験手順

To a cooled solution (-78° C.) of oxalyl chloride (3.06 mL, 35.1 mmol, 2 eq) in methylene chloride (100 mL) under nitrogen was added distilled dimethylsulfoxide (5.00 mL, 70.2 mmol, 4 eq). After 10 min 1-(2-chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl) piperidin-4-ol (described in example 11) (5.96 g, 17.5 mmol) was added as a methylene chloride solution (10 mL). The reaction was stirred at -78° C. for 30 min prior to the addition of triethylamine (19.6 mL, 140 mmol, 8 eq). The cooling bath was removed and the reaction warmed to room temperature over 1.5 h. The reaction was poured into 2.5N NaOH (100 mL) and the aqueous phase extracted with methylene chloride (3×100 mL). Combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and reduced to an oil. The crude reaction mixture was purified by flash chromatography over silica gel (400 mL, eluent: 20% ethyl acetate in hexane) to yield 5.53 g (93%) of the title compound. TLC analysis (Rf 0.21, 20% ethyl acetate in hexane). 1H NMR (CDCl3, 250 MHz) 7.26 (m, 1H), 7.13 (m, 3H), 6.95 (m, 3H), 4.28 (s, 1H), 3.49 (s, 2H), 2.94 (t, J=6.1 Hz, 4H), 2.62 (s, 2H), 2.43 (t, J=6.0 Hz, 4H) MS (CI, CH4) m/z 338 (M+1,100), 340 (35), 366 (M+29,31).

後処理

  1. customThe cooling bath was removed
  2. temperaturethe reaction warmed to room temperature over 1.5 h
  3. additionThe reaction was poured into 2.5N NaOH (100 mL)
  4. extractionthe aqueous phase extracted with methylene chloride (3×100 mL)
  5. dry with materialCombined organic extracts were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customThe crude reaction mixture
  8. customwas purified by flash chromatography over silica gel (400 mL, eluent: 20% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-be364fe4248a46d5b62dfa8870f4e619
出典データセット
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05512575

反応ノート

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