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Sodium Carbonate → methyl 6-(2-fluorocyclohexyl)-5-(2-formylphenyl)-4-(2-methoxy-2-oxoethyl)-4H-thieno[3,2-b]pyrrole-2-carboxylate

HRID 1008992
ノート
印刷プレビュー

反応式

HRID 1008992 の反応式
Br[C:2]1[N:6]([CH2:7][C:8]([O:10][CH3:11])=[O:9])[C:5]2[CH:12]=[C:13]([C:15]([O:17][CH3:18])=[O:16])[S:14][C:4]=2[C:3]=1[CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[F:25].[CH:26]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1B(O)O)=[O:27].C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1.CCOC(C)=O.[Cl-].[Na+].O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[F:25][CH:20]1[CH2:21][CH2:22][CH2:23][CH2:24][CH:19]1[C:3]1[C:4]2[S:14][C:13]([C:15]([O:17][CH3:18])=[O:16])=[CH:12][C:5]=2[N:6]([CH2:7][C:8]([O:10][CH3:11])=[O:9])[C:2]=1[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][C:28]=1[CH:26]=[O:27]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 10340Sodium CarbonateHCID 2921892-Formylphenylboronic acidHCID 67298644HCID 67298644、化合物

生成物 1

HCID 86629784methyl 6-(2-fluorocyclohexyl)-5-(2-formylphenyl)-4-(2-methoxy-2-oxoethyl)-4H-thieno[3,2-b]pyrrole-2-carboxylate収率 56%

試薬・触媒・溶媒 4

HCID 178418397
HCID 178418397、化合物
触媒
HCID 8857Ethyl Acetate溶媒
HCID 312751,4-Dioxane溶媒
HCID 57417360Sodium chloride; water溶媒

実験手順

A solution (0.1 M) of methyl 5-bromo-6-(2-fluorocyclohexyl)-4-(2-methoxy-2-oxoethyl)-4H-thieno[3,2-b]pyrrole-2-carboxylate in dioxane was treated with (2-formylphenyl)boronic acid (1.5 eq.); aq. Na2CO3-solution (2 N, 8.5 eq.) was added and the solution was degassed, and then treated with Pd(PPh3)4 (0.1 eq.). A balloon with argon was installed, the mixture was placed in an oil bath preheated at 115° C. and stirred for 30 min, then cooled and diluted with EtOAc and brine. The organic phase was separated, washed with 1N HCl and brine, dried and concentrated. The residue was purified by chromatography (PE/EtOAc) to give the title compound (56%); some starting material (21%) was recovered. 1H-NMR (400 MHz, CDCl3, 300K, δ) 9.78&9.85* (bs, 1H.), 8.06 (dd, 1H, J 7.7, 1.3), 7.67 (s, 1H), 7.73-7.60 (m, 2H), 7.44 (bd, 1H, J 7.5), 4.50&4.55* (d, 1H, J 17.8&17.6), 4.44&4.48* (d, 1H, J 17.8&17.6), 4.73-4.49 (m, 1H), 3.91 (s, 3H), 3.62&3.63* (s, 3H), 2.42-2.34 (m, 1H), 2.18-2.12 (m, 1H), 1.83-1.07 (m, 7H); MS (ES+) m/z 458 (M+H)+. * Refers to two different conformers.

後処理

  1. customthe solution was degassed
  2. customthe mixture was placed in an oil bath
  3. custompreheated at 115° C.
  4. temperaturecooled
  5. customThe organic phase was separated
  6. washwashed with 1N HCl and brine
  7. customdried
  8. concentrationconcentrated
  9. customThe residue was purified by chromatography (PE/EtOAc)

出典と根拠

ORDレコード
ord-6c3efd7dd30e40d39e6807c564465ed7
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07973026B2

反応ノート

読み込み中…

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