ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

1,2-Dimethoxyethane → Methyl 4-(2-aminopyridin-3-yl)-2-methylbenzoate

HRID 596080
ノート
印刷プレビュー

反応式

HRID 596080 の反応式
CC1(C)C(C)(C)OB([C:9]2[C:10]([NH2:15])=[N:11][CH:12]=[CH:13][CH:14]=2)O1.Br[C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[C:20]([CH3:28])[CH:19]=1.COCCOC.C([O-])([O-])=O.[Na+].[Na+]>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl.CCCCCCC.CCOCC>[NH2:15][C:10]1[C:9]([C:18]2[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[C:20]([CH3:28])[CH:19]=2)=[CH:14][CH:13]=[CH:12][N:11]=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 80711,2-DimethoxyethaneHCID 10340Sodium CarbonateHCID 22031226Methyl 4-bromo-2-methylbenzoateHCID 438110672-Aminopyridine-3-boronic acid, pinacol ester

生成物 1

HCID 118046459Methyl 4-(2-aminopyridin-3-yl)-2-methylbenzoate収率 62.1%

試薬・触媒・溶媒 3

HCID 178418807
HCID 178418807、化合物
触媒
HCID 3283Diethyl Ether溶媒
HCID 8900Heptane溶媒

反応条件

温度
108 °C

実験手順

To 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine(7.37 g, 33.5 mmol) in 500 mL round bottom flask were added methyl 4-bromo-2-methylbenzoate (6.390 g, 27.9 mmol), PdCl2(dppf)-DCM (2.041 g, 2.79 mmol), DME (209 mL) and 2 M Na2CO3 solution (69.7 mL). The reaction mixture was bubbled through N2 for 20 min and heated in an oil bath at 108° C. for 1.5 h. The reaction mixture was diluted with EtOAc, washed with water three times, dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography eluting with 0-100% of EtOAc (containing 10% of MeOH)/heptane to provide crude product around 8 g which contained fair amount of B2(PIN)2 from previous experiment. Ether was added to dissolve the crude mixture, and then heptane was added to crush out the desired product. Solid was filtered out to provide 4.2 g of desired product with high purity in 62.1% yield. LCMS (m/z): 243.5 (MH+), 0.56 min.

後処理

  1. customThe reaction mixture was bubbled through N2 for 20 min
  2. additionThe reaction mixture was diluted with EtOAc
  3. washwashed with water three times
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by flash chromatography
  8. washeluting with 0-100% of EtOAc (containing 10% of MeOH)/heptane
  9. customto provide crude product around 8 g which

出典と根拠

ORDレコード
ord-e08fcfd5f86c4dfaa9ca0ddc469a300a
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242996B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート