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HCID 67281758、化合物 → HCID 67282524、化合物

HRID 1187502
ノート
印刷プレビュー

反応式

HRID 1187502 の反応式
C([O:8][C:9]1[C:14](=[O:15])[C:13]([CH2:16][C:17]([F:20])([F:19])[F:18])=[CH:12][N:11]([CH3:21])[C:10]=1[CH3:22])C1C=CC=CC=1.[H][H]>CO.[Pd]>[OH:8][C:9]1[C:14](=[O:15])[C:13]([CH2:16][C:17]([F:20])([F:18])[F:19])=[CH:12][N:11]([CH3:21])[C:10]=1[CH3:22]
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 2

HCID 67281758HCID 67281758、化合物HCID 178418361HCID 178418361、化合物

生成物 1

HCID 67282524HCID 67282524、化合物収率 69%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒2 回

実験手順

A clear solution of 3-benzyloxy-1,2-dimethyl-5-(2,2,2-trifluoro-ethyl)-1H-pyridin-4-one (1.1 g, 3.53 mmol) in methanol (32 mL) was debenzylated using Pd/C (10 wt. %, dry basis, on activated carbon, wet, Degussa type E101 NE/W, 0.17 g) as catalyst in a hydrogen atmosphere at a pressure of 50 psi for 30 min. The reaction mixture was diluted with methanol (30 mL), and sonicated for 10 min. A CELITE™ bed was prepared on a sintered glass, and washed with 6M HCl (100 mL), followed by water (7×50 mL) and then methanol (2×50 mL) under suction. The reaction mixture was filtered through the pre-treated CELITE™ bed. The volume of the filtrate was reduced to about 20 mL by evaporation under reduced pressure. HPLC analysis (HPLC Method 1, Example 24) of the filtrate indicated the presence of about 42% (peak percent area) of the starting material. Another 150 mg of Pd/C was added, and the mixture was subjected to the debenzylation reaction condition for a further 20 min, and worked up as described above. The catalyst was filtered off, and the filtrate was evaporated to dryness to afford 3-hydroxy-1,2-dimethyl-5-(2,2,2-trifluoro-ethyl)-1H-pyridin-4-one as a solid product (0.54 g, 69% yield, HPLC Method 1 (Example 24), RT=9.9 min, HPLC purity (peak percent area): 99.3% at λ=280 nm). 1H NMR (DMSO-d5) δ ppm: 7.70 (s, 1H), 3.65 (s, 3H), 3.39 (q, J=11.5 Hz, 2H), 2.26 (s, 3H). MS-ESI (m/z) 222.2 ([M+1]+, 100%), 202.2, 182.2.

後処理

  1. customfor 30 min
  2. customsonicated for 10 min
  3. customA CELITE™ bed was prepared on a sintered glass
  4. washwashed with 6M HCl (100 mL)
  5. filtrationThe reaction mixture was filtered through the pre-treated CELITE™ bed
  6. customThe volume of the filtrate was reduced to about 20 mL by evaporation under reduced pressure
  7. additionAnother 150 mg of Pd/C was added
  8. customthe mixture was subjected to the debenzylation reaction condition for a further 20 min
  9. filtrationThe catalyst was filtered off
  10. customthe filtrate was evaporated to dryness

出典と根拠

ORDレコード
ord-4fa4b9fda53b4d5f9284fcd16e136e78
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08673943B2

反応ノート

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