Hydrochloric Acid → 2-(4-{5-[2-(2-Fluoro-phenyl)-[1,8]naphthyridin-4-yl]-pyridin-3-yl}-pyrazol-1-yl)-ethanol

HRID 1404304ノート

反応式

HRID 1404304 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:17]=[C:16]([C:18]2[CH:19]=[N:20][CH:21]=[C:22]([C:24]3[CH:25]=[N:26][N:27]([CH2:29][CH2:30][O:31]C4CCCCO4)[CH:28]=3)[CH:23]=2)[C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[N:9]=1.Cl>ClCCl.O1CCOCC1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:17]=[C:16]([C:18]2[CH:23]=[C:22]([C:24]3[CH:25]=[N:26][N:27]([CH2:29][CH2:30][OH:31])[CH:28]=3)[CH:21]=[N:20][CH:19]=2)[C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[N:9]=1

参加物

5

実験手順

A solution of 219 mg (0.44 mmol) 2-(2-fluoro-phenyl)-4-(5-{1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-pyrazol-4-yl}-pyridin-3-yl)-[1,8]naphthyridine in 7 ml dichloromethane was treated with 0.52 ml of a 4 N solution of hydrochloric acid in dioxane. The reaction mixture was stirred for 60 minutes and the precipitate that had formed was filtered off. The residue was dissolved in water and treated with saturated sodium carbonate solution. The resulting precipitate was filtered off, washed with water and dried under vacuum yielding 2-(4-{5-[2-(2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-pyridin-3-yl}-pyrazol-1-yl)-ethanol as colorless crystals; HPLC-MS: 1.70 min, [M+H] 412.

後処理

  1. customthe precipitate that had formed
  2. filtrationwas filtered off
  3. dissolutionThe residue was dissolved in water
  4. additiontreated with saturated sodium carbonate solution
  5. filtrationThe resulting precipitate was filtered off
  6. washwashed with water
  7. customdried under vacuum

出典と根拠

ORDレコード
ord-e109f756033644d5b7d32214306606e7
出典データセット
uspto-grants-2014_12
特許番号
US08912216B2

反応ノート

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