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Water → Methyl 2-methoxy-6-(pyrimidin-2-yl)benzoate

HRID 869013
ノート
印刷プレビュー

反応式

HRID 869013 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9](B2OC(C)(C)C(C)(C)O2)[C:4]=1[C:5]([O:7][CH3:8])=[O:6].Br[C:23]1[N:28]=[CH:27][CH:26]=[CH:25][N:24]=1.C([O-])([O-])=O.[Na+].[Na+].O>C1COCC1.CC(P(C(C)(C)C)[C-]1C=CC=C1)(C)C.CC(P(C(C)(C)C)[C-]1C=CC=C1)(C)C.Cl[Pd]Cl.[Fe+2].CCOC(C)=O>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([C:23]2[N:28]=[CH:27][CH:26]=[CH:25][N:24]=2)[C:4]=1[C:5]([O:7][CH3:8])=[O:6]
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 962Water2 回HCID 10340Sodium CarbonateHCID 783452-BromopyrimidineHCID 56776719Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

生成物 1

HCID 90411951Methyl 2-methoxy-6-(pyrimidin-2-yl)benzoate収率 63.4%

試薬・触媒・溶媒 3

HCID 178454861
HCID 178454861、化合物
触媒
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

In a microwave vial was dissolved methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (CAS 1146214-77-8) (500 mg, 1.71 mmol) and 2-bromopyrimidine (344 mg, 2.05 mmol) in THF (8.5 mL). Na2CO3 (544 mg, 5.14 mmol) was then added followed by water (4 mL) and the reaction mixture was degassed with N2 for 10 minutes. PdCl2(dtbpf) (CAS 95408-45-0) (45 mg, 0.069 mmol) was then added and the reaction mixture was heated at 80° C. for 4 h. The mixture was cooled to room temperature and water and EtOAc added. The reaction mixture was extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4, filtered and concentrated. The crude was purified via silica gel chromatography (0-70% EtOAc in hexanes) to afford the title compound (265 mg, 63%). MS (ESI) mass calcd. for C13H12N2O3, 244.1. m/z found 245.1 [M+H]+. 1H NMR (400 MHz, Chloroform-d) δ 8.78 (d, J=4.9 Hz, 2H), 7.99 (dd, J=7.9, 0.9 Hz, 1H), 7.49 (t, J=8.1 Hz, 1H), 7.19 (t, J=4.8 Hz, 1H), 7.09 (dd, J=8.3, 0.9 Hz, 1H), 3.90 (s, 3H), 3.89 (s, 3H).

後処理

  1. customthe reaction mixture was degassed with N2 for 10 minutes
  2. temperatureThe mixture was cooled to room temperature
  3. extractionThe reaction mixture was extracted with EtOAc (3×)
  4. dry with materialThe combined organic layers were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude was purified via silica gel chromatography (0-70% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-6b602650c4e04e47b119d152d4718c2f
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969352B2

反応ノート

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