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Dimethyl[5-(benzyloxy)-1-(biphenyl-3-yl)-4-oxo-1,4-dihydropyridin-3-yl]boronate → [1-(Biphenyl-3-yl)-5-hydroxy-4-oxo-1,4-dihydropyridin-3-yl]boronic acid

HRID 571052
ノート
印刷プレビュー

反応式

HRID 571052 の反応式
C[O:2][B:3]([C:6]1[C:11](=[O:12])[C:10]([O:13]CC2C=CC=CC=2)=[CH:9][N:8]([C:21]2[CH:22]=[C:23]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[CH:24]=[CH:25][CH:26]=2)[CH:7]=1)[O:4]C>C1COCC1.CO.CO.[Pd]>[C:23]1([C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:24]=[CH:25][CH:26]=[C:21]([N:8]2[CH:9]=[C:10]([OH:13])[C:11](=[O:12])[C:6]([B:3]([OH:2])[OH:4])=[CH:7]2)[CH:22]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 67404775Dimethyl[5-(benzyloxy)-1-(biphenyl-3-yl)-4-oxo-1,4-dihydropyridin-3-yl]boronate

生成物 1

HCID 53379376[1-(Biphenyl-3-yl)-5-hydroxy-4-oxo-1,4-dihydropyridin-3-yl]boronic acid

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒HCID 21899815MeOH tetrahydrofuran溶媒

実験手順

Lithium chloride (515 mg, 12.1 mmol) in a 25 mL round bottom flask under high vacuum was heated with a heat gun until a free flowing granular solid was obtained (˜5 min). The flask was cooled to room temperature, purged with N2, and treated with isopropylmagnesium chloride (6.1 mL of a 2 M solution in THF). After stirring at room temperature for 1 h, the mixture was cooled to −10° C. and treated with 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one (1.05 g, 2.4 mmol) as a suspension in 3.5 mL of THF. After stirring for 0.5 h, trimethylborate (1.35 mL, 12.1 mmol) was added dropwise and the reaction mixture was stirred an additional 3.5 h, before being quenched with the addition of MeOH (12 mL) to provide a solution of crude dimethyl[5-(benzyloxy)-1-(biphenyl-3-yl)-4-oxo-1,4-dihydropyridin-3-yl]boronate which was used directly in the subsequent step. LC/MS (M+H)+ 398. The solution of crude dimethyl[5-(benzyloxy)-1-(biphenyl-3-yl)-4-oxo-1,4-dihydropyridin-3-yl]boronate (2.4 mmol) in THF/MeOH from the preceeding step and 10% Pd/C (52 mg, 0.49 mmol) was stirred under H2 (1 atm) for 18 h. The reaction mixture was diluted with MeOH (20 mL), filtered through a pad of Celite (MeOH wash), and concentrated under reduced pressure. The residue was diluted with DMF (10 mL) and 0.5 M aq, HCl (0.4 mL) and purified by reversed phase HPLC (2 cm×5 cm C18, acetonitrile-water gradient, 0.05% TFA added, fractions were lypholized) to provide [1-(biphenyl-3-yl)-5-hydroxy-4-oxo-1,4-dihydropyridin-3-yl]boronic acid. 1H NMR (599 MHz, DMSO, 75° C.): δ 8.19 (d, J=2.3 Hz, 1 H); 7.89 (d, J=2.3 Hz, 1 H); 7.83 (s, 1 H); 7.79-7.74 (m, 3 H); 7.67-7.61 (m, 1 H); 7.56 (d, J=8.1 Hz, 1 H); 7.49 (t, J=7.6 Hz, 2 H); 7.46-7.38 (m, 1 H). HRMS (ES) Calc (M+H)+ 308.1089. Found 308.1092.

後処理

  1. filtrationfiltered through a pad of Celite (MeOH wash)
  2. concentrationconcentrated under reduced pressure
  3. additionThe residue was diluted with DMF (10 mL) and 0.5 M aq
  4. customHCl (0.4 mL) and purified by reversed phase HPLC (2 cm×5 cm C18, acetonitrile-water gradient, 0.05% TFA added, fractions were lypholized)

出典と根拠

ORDレコード
ord-4a23b0633ac24a19b2753eeb0162545e
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09024032B2

反応ノート

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