HCID 178452591、化合物 → HCID 178507125、化合物

HRID 1509078ノート

反応式

HRID 1509078 の反応式
C(OC(=O)[NH:7][C:8]1([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[C:27]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)=[CH:26][C:25]4[C:24]5=[N:34][NH:35][C:36]([OH:37])=[C:23]5[CH2:22][CH2:21][C:20]=4[N:19]=3)=[CH:14][CH:13]=2)[CH2:11][CH2:10][CH2:9]1)(C)(C)C>C(O)(C(F)(F)F)=O>[NH2:7][C:8]1([C:12]2[CH:13]=[CH:14][C:15]([C:18]3[C:27]([C:28]4[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=4)=[CH:26][C:25]4[C:24]5=[N:34][NH:35][C:36]([OH:37])=[C:23]5[CH2:22][CH2:21][C:20]=4[N:19]=3)=[CH:16][CH:17]=2)[CH2:11][CH2:10][CH2:9]1

参加物

3

実験手順

tert-butyl(1-(4-(3-hydroxy-8-phenyl-4,5-dihydro-2H-pyrazolo[3,4-f]quinolin-7-yl)phenyl)cyclobutyl)carbamate (19 mg, 0.037 mmol) was dissolved in TFA (1 mL) and stirred for 30 seconds. The solution was immediately concentrated to dryness under reduced pressure. The residue was dissolved in diethyl ether (˜2 mL) and concentrated to dryness under reduced pressure three times. The residue was then slurried in diethyl ether (2 mL) and after settling the supernatant solvent removed by pipette. This was repeated three times. The remaining solvent was removed under reduced pressure and dried to give the desired product as an off-white solid (3 mg, 17% yield). 1H-NMR (500 MHz, CD3OD) δ 8.05 (1H, s), 7.49 (2H, d), 7.44 (2H, d), 7.27-7.34 (3H, m), 7.20-7.27 (2H, m), 3.25 (2H, t), 2.87 (2H, t), 2.72-2.82 (2H, m), 2.54-2.65 (2H, m), 2.18-2.30 (1H, m), 1.90-2.03 (1H, m). LCMS (Method A) RT=3.40 min, M+H+=409.19.

後処理

  1. concentrationThe solution was immediately concentrated to dryness under reduced pressure
  2. dissolutionThe residue was dissolved in diethyl ether (˜2 mL)
  3. concentrationconcentrated to dryness under reduced pressure three times
  4. customremoved by pipette
  5. customThe remaining solvent was removed under reduced pressure
  6. customdried

出典と根拠

ORDレコード
ord-d1b4005032204779981f14dcc89348b5
出典データセット
uspto-grants-2015_12
特許番号
US09221838B2

反応ノート

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