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Diisopropylethylamine → Tert-butyl (+/-)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate

HRID 2281157
ノート
印刷プレビュー

反応式

HRID 2281157 の反応式
[CH3:1][CH:2]([CH3:19])[CH2:3][C:4]([C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1)=O.[CH3:20][C:21]1[CH:22]=[N+:23]([O-])[C:24]2[C:29]([CH:30]=1)=[CH:28][CH:27]=[CH:26][CH:25]=2.C([N:35](C(C)C)CC)(C)C.F[P-](F)(F)(F)(F)F.Br[P+](N1CCCC1)(N1CCCC1)N1CCCC1>ClCCl.C(=O)(O)[O-].[Na+]>[CH3:1][CH:2]([CH3:19])[CH2:3][CH:4]([C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1)[NH:35][C:22]1[C:21]([CH3:20])=[CH:30][C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[N:23]=1
参加物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 81531DiisopropylethylamineHCID 2733179PyBroPHCID 70214663-Methylquinoline N-oxideHCID 71239698Tert-butyl 4-(3-methylbutanoyl)benzoate

生成物 1

HCID 71243814Tert-butyl (+/-)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate

試薬・触媒・溶媒 2

HCID 6344
Dichloromethane
溶媒
HCID 516892Sodium Bicarbonate溶媒

実験手順

To a solution of tert-butyl (+/−)-4-(3-methylbutanoyl)benzoate (527 mg, 2.00 mmol) and 3-methylquinoline N-oxide (318 mg, 2.00 mmol) in dichloromethane (8.0 mL) was added diisopropylethylamine (1.31 mL, 7.50 mmol) followed by bromotripyrrolidinophosphonium hexafluorophosphate (1.18 g, 2.50 mmol). The solution was stirred at room temperature for 18 hours then diluted with sat. aq sodium bicarbonate (20 mL). The mixture was extracted with ethyl acetate (3×20 mL). The combined organics were dried over anhydrous Na2SO4 and filtered, and the filtrate was concentrated. Purification by silica gel flash chromatography (ethyl acetate/heptane) gave tert-butyl (+/−)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.94 (d, J=8.2 Hz, 2 H), 7.63 (d, J=8.2 Hz, 1 H), 7.59 (s, 1 H), 7.54-7.48 (m, 3 H), 7.47-7.41 (m, 1 H), 7.19-7.13 (m, 1 H), 5.56 (q, J=7.4 Hz, 1 H), 4.73 (d, J=7.0 Hz, 1 H), 2.28 (s, 3 H), 1.94-1.83 (m, 1 H), 1.81-1.70 (m, 1 H), 1.70-1.60 (m, 1 H), 1.57 (s, 9 H), 1.04 (d, J=6.6 Hz, 3 H), 0.97 (d, J=6.6 Hz, 3 H).

後処理

  1. extractionThe mixture was extracted with ethyl acetate (3×20 mL)
  2. dry with materialThe combined organics were dried over anhydrous Na2SO4
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated
  5. customPurification by silica gel flash chromatography (ethyl acetate/heptane)

出典と根拠

ORDレコード
ord-ef581192a10e41cdaac9472e07d6e500
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09139538B2

反応ノート

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