Tritium → methyl (S)-5-cyclobutoxy-6-(5-fluoro-1-(piperidin-4-yl)-1H-pyrazol-4-yl)-2-methyl-3,4-dihydroquinoline-1(2H)-carboxylate

HRID 1051743ノート

反応式

HRID 1051743 の反応式
[H][H].C([N:10]1[CH2:15][CH2:14][CH:13]([N:16]2[C:20]([F:21])=[C:19]([C:22]3[C:23]([O:37][CH:38]4[CH2:41][CH2:40][CH2:39]4)=[C:24]4[C:29](=[CH:30][CH:31]=3)[N:28]([C:32]([O:34][CH3:35])=[O:33])[C@@H:27]([CH3:36])[CH2:26][CH2:25]4)[CH:18]=[N:17]2)[CH2:12][CH2:11]1)C1C=CC=CC=1.[3H][3H]>CO.[OH-].[OH-].[Pd+2]>[CH:38]1([O:37][C:23]2[C:22]([C:19]3[CH:18]=[N:17][N:16]([CH:13]4[CH2:14][CH2:15][NH:10][CH2:11][CH2:12]4)[C:20]=3[F:21])=[CH:31][CH:30]=[C:29]3[C:24]=2[CH2:25][CH2:26][C@H:27]([CH3:36])[N:28]3[C:32]([O:34][CH3:35])=[O:33])[CH2:39][CH2:40][CH2:41]1

参加物

6

反応物 3

HCID 24824TritiumHCID 118075772(S)-methyl 6-(1-(1-benzylpiperidin-4-yl)-5-fluoro-1H-pyrazol-4-yl)-5-cyclobutoxy-2-methyl-3,4-dihydroquinoline-1(2H)-carboxylateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 118086342methyl (S)-5-cyclobutoxy-6-(5-fluoro-1-(piperidin-4-yl)-1H-pyrazol-4-yl)-2-methyl-3,4-dihydroquinoline-1(2H)-carboxylate収率 58.1%

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒HCID 887Methanol溶媒

実験手順

Balloon filled hydrogen was charged into a nitrogen purged suspension of (S)-methyl 6-(1-(1-benzylpiperidin-4-yl)-5-fluoro-1H-pyrazol-4-yl)-5-cyclobutoxy-2-methyl-3,4-dihydroquinoline-1(2H)-carboxylate (15.0 mg, 0.028 mmol) and 20% palladium hydroxide on carbon (40 mg, 0.285 mmol) in methanol (10 mL). The reaction flask was backfilled with hydrogen 3 times. The reaction solution was then stirred under a hydrogen atmosphere for 2 hours. The flask was purged with nitrogen, and the reaction mixture was filtered through of Celite and the bed of Celite was washed with ethyl acetate (10 mL). The filtered solvent was then concentrated in vacuo. The crude product was added directly to a plug of silica gel and eluted with 30% ethyl acetate in methanol to afford methyl (S)-5-cyclobutoxy-6-(5-fluoro-1-(piperidin-4-yl)-1H-pyrazol-4-yl)-2-methyl-3,4-dihydroquinoline-1(2H)-carboxylate (7.2 mg, 58%) as an off-white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.09 (d, J=6.45 Hz, 3H), 1.21-1.30 (m, 2H), 1.42-1.57 (m, 1H), 1.76-1.88 (m, 3H), 1.89-2.01 (m, 5H), 2.34-2.43 (m, 2H), 2.53-2.61 (m, 1H), 2.71-2.85 (m, 2H), 3.03 (br d, J=12.31 Hz, 1H), 3.13-3.21 (m, 1H), 3.68 (s, 3H), 3.95-4.05 (m, 1H), 4.15-4.30 (m, 1H), 4.41-4.52 (m, 1H), 7.14 (d, J=8.15 Hz, 1H), 7.29 (d, J=8.79 Hz, 1H), 7.61 (s, 1H). MS (ESI, pos. ion) m/z 443 [M+H]+.

後処理

  1. additionwas charged into a nitrogen
  2. custompurged
  3. customThe flask was purged with nitrogen
  4. filtrationthe reaction mixture was filtered through of Celite
  5. washthe bed of Celite was washed with ethyl acetate (10 mL)
  6. concentrationThe filtered solvent was then concentrated in vacuo
  7. additionThe crude product was added directly to a plug of silica gel
  8. washeluted with 30% ethyl acetate in methanol

出典と根拠

ORDレコード
ord-7aefbbddab3d4d329b375299a9566408
出典データセット
uspto-grants-2016_07
特許番号
US09388161B2

反応ノート

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