Tetrahydrofuran → HCID 23509023、化合物

HRID 1884253ノート

反応式

HRID 1884253 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:17][CH2:18][NH2:19])[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(N(CC)CC)C.O1CCCC1.[CH:32]1[C:41]2[CH2:40][CH2:39][CH2:38][CH2:37][C:36]=2[CH:35]=[CH:34][C:33]=1[CH2:42][C:43](Cl)=[O:44]>O>[CH2:10]([O:9][C:8]1[CH:7]=[CH:6][C:5]([CH2:17][CH2:18][NH:19][C:43](=[O:44])[CH2:42][C:33]2[CH:34]=[CH:35][C:36]3[CH2:37][CH2:38][CH2:39][CH2:40][C:41]=3[CH:32]=2)=[CH:4][C:3]=1[O:2][CH3:1])[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1

参加物

6

反応物 4

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 200382Phenethylamine, 4-(benzyloxy)-3-methoxy-HCID 23508965(5,6,7,8-Tetrahydronaphthalen-2-yl)acetyl chloride

生成物 1

HCID 23509023HCID 23509023、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

8.01 g (31.2 mmol) of crude 2-(3-methoxy-4-benzyloxyphenyl)ethylamine, 3.78 g (37.4 mmol) of triethylamine and 80 ml of tetrahydrofuran were mixed and cooled to 0° C. and then (5,6,7,8-tetrahydronaphthalen-2-yl)acetyl chloride was added dropwise thereto. The mixture was stirred at 0° C. for 30 minutes and further at room temperature for 2 hours. Water was added to the reaction mixture, which was followed by extracted with ethyl acetate, washed with 5% hydrochloric acid and then saturated brine, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (eluent, hexane:ethyl acetate=1:1) to give 8.3 g of N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetamide.

後処理

  1. extractionby extracted with ethyl acetate
  2. washwashed with 5% hydrochloric acid
  3. dry with materialsaturated brine, dried over anhydrous magnesium sulfate
  4. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-b9be2b3a757c49ffa25f02056c42ac50
出典データセット
uspto-grants-2004_07
特許番号
US06762321B2

反応ノート

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