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Benzyl piperazine-1-carboxylate → Benzyl 4-(2-(benzyloxy)pyridin-3-yl)piperazine-1-carboxylate

HRID 1804619
ノート
印刷プレビュー

反応式

HRID 1804619 の反応式
C1(P(C2CCCCC2)C2C=CC=CC=2C2C(N(C)C)=CC=CC=2)CCCCC1.[CH2:29]([O:36][C:37]1[C:42](Br)=[CH:41][CH:40]=[CH:39][N:38]=1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.[N:44]1([C:50]([O:52][CH2:53][C:54]2[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=2)=[O:51])[CH2:49][CH2:48][NH:47][CH2:46][CH2:45]1.CC(C)([O-])C.[Na+]>C1(C)C=CC=CC=1.O.C1(/C=C/C(=O)/C=C/C2C=CC=CC=2)C=CC=CC=1.[Pd]>[CH2:29]([O:36][C:37]1[C:42]([N:47]2[CH2:46][CH2:45][N:44]([C:50]([O:52][CH2:53][C:54]3[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=3)=[O:51])[CH2:49][CH2:48]2)=[CH:41][CH:40]=[CH:39][N:38]=1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=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

8

反応物 4

HCID 643495Benzyl piperazine-1-carboxylateHCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 147124562-Benzyloxy-3-bromopyridineHCID 23676156Sodium t-butoxide

生成物 1

HCID 67060675Benzyl 4-(2-(benzyloxy)pyridin-3-yl)piperazine-1-carboxylate収率 55%

試薬・触媒・溶媒 3

HCID 15673654
(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladium
触媒
HCID 962Water溶媒
HCID 1140Toluene溶媒

反応条件

温度
80 °C

実験手順

To a stirred suspension of 0.011 g (0.012 mmol) of (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium (3:2) in 3 mL of anhydrous toluene under an atmosphere of nitrogen was added 0.015 g (0.037 mmol) of 2′-(dicyclohexylphosphino)-N,N-dimethylbiphenyl-2-amine and the resulting mixture was allowed to stir for 20 min. Next, 0.11 g (0.41 mmol) of 2-(benzyloxy)-3-bromopyridine was added followed by 0.11 g (0.49 mmol) of benzyl piperazine-1-carboxylate and 0.059 g (0.61 mmol) of sodium tert-butoxide. The resulting mixture was then heated to 80° C. overnight. After cooling to ambient temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with water then brine, dried over magnesium sulfate and evaporated to dryness in vacuo. The residue was purified by silica gel chromatography eluting with a 0-100% acetone in hexanes gradient to afford the title compound as clear gum (0.090 g, 55%). 1H-NMR (500 MHz, CDCl3) δ 7.84 (dd, J=4.9, 1.6 Hz, 1H), 7.47-7.29 (m, 10H), 7.09 (dd, J=7.5, 1.6 Hz, 1H), 6.87 (dd, J=7.5, 4.9 Hz, 1H), 5.46 (s, 2H), 5.16 (s, 2H), 3.67-3.65 (m, 4H), 3.07 (br s, 4H). LC-MS: m/z (ES) 404.0 (MH)+.

後処理

  1. temperatureAfter cooling to ambient temperature
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layers were washed with water
  4. dry with materialbrine, dried over magnesium sulfate
  5. customevaporated to dryness in vacuo
  6. customThe residue was purified by silica gel chromatography
  7. washeluting with a 0-100% acetone in hexanes gradient

出典と根拠

ORDレコード
ord-c69d606ce85b4564ae29aa1d539c9d58
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08354403B2

反応ノート

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