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Triethylamine → 2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester

HRID 858366
ノート
印刷プレビュー

反応式

HRID 858366 の反応式
C(Cl)(=O)C(C)(C)C.[CH2:8]([O:10][C:11]1[CH:12]=[C:13]([CH2:22][C:23]([OH:25])=O)[CH:14]=[CH:15][C:16]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH3:9].C(N(CC)CC)C.[CH3:33][CH:34]([CH3:50])[CH2:35][C@H:36]([NH2:49])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1[N:43]1[CH2:48][CH2:47][CH2:46][CH2:45][CH2:44]1>C1(C)C=CC=CC=1.CCCCCC>[CH2:8]([O:10][C:11]1[CH:12]=[C:13]([CH2:22][C:23]([NH:49][C@H:36]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=2[N:43]2[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48]2)[CH2:35][CH:34]([CH3:50])[CH3:33])=[O:25])[CH:14]=[CH:15][C:16]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH3:9]
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

7

反応物 4

HCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 101312123-Ethoxy-4-ethoxycarbonylphenylacetic acidHCID 105146093-Methyl-1-(2-piperidinophenyl)-1-butylamine, (S)-

生成物 1

HCID 106484192-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester収率 73%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒3 回HCID 8058Hexane溶媒

反応条件

温度
30 °C

実験手順

Pivaloyl chloride (5.4 g, 45 mmol) was added to a mixture of 3-ethoxy-4-ethoxycarbonyl phenylacetic acid (10.0 g, 40 mmol), toluene (50 ml) and triethylamine (5.0 g, 49 mmol) at −5° C. and stirred for 1 hour. A solution of (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine (9.8 g, 40 mmol) in toluene (20 ml) was then added at below 10° C. The temperature of the reaction mixture was raised to 30° C. and the mixture stirred overnight. It was then washed with water and saturated sodium bicarbonate solution. Toluene was distilled off under reduced pressure to get the crude product. The crude product was dissolved in toluene (35 ml), hexane (200 ml) was added and the mixture cooled at 0° C. The solid product so obtained was filtered and dried to give 14.0 g of the title compound (Yield: 73%, HPLC Purity 99%).

後処理

  1. stirringthe mixture stirred overnight
  2. washIt was then washed with water and saturated sodium bicarbonate solution
  3. distillationToluene was distilled off under reduced pressure
  4. customto get the crude product
  5. temperaturethe mixture cooled at 0° C
  6. customThe solid product so obtained
  7. filtrationwas filtered
  8. customdried

出典と根拠

ORDレコード
ord-f8329fcb31f64a37ba5427f9c5fdadb5
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07148355B2

反応ノート

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