Acetic Acid → 7-(1-Cyclopropylmethyl-piperidin-4-yloxy)-3,4-dihydro-2H-2,4a,5-triaza-fluoren-1-one

HRID 506748ノート

反応式

HRID 506748 の反応式
[NH:1]1[CH2:6][CH2:5][CH:4]([O:7][C:8]2[CH:20]=[C:19]3[C:11]([N:12]4[C:17](=[CH:18]3)[C:16](=[O:21])[NH:15][CH2:14][CH2:13]4)=[N:10][CH:9]=2)[CH2:3][CH2:2]1.O.[CH:23]1([CH:26]=O)[CH2:25][CH2:24]1.C(O)(=O)C.C([BH3-])#N.[Na+].C(=O)(O)[O-].[Na+]>O1CCCC1>[CH:23]1([CH2:26][N:1]2[CH2:2][CH2:3][CH:4]([O:7][C:8]3[CH:20]=[C:19]4[C:11]([N:12]5[C:17](=[CH:18]4)[C:16](=[O:21])[NH:15][CH2:14][CH2:13]5)=[N:10][CH:9]=3)[CH2:5][CH2:6]2)[CH2:25][CH2:24]1

参加物

8

反応条件

温度
55 °C

実験手順

To a solution of 0.40 g (1.40 mmol) 7-(piperidin-4-yloxy)-3,4-dihydro-2H-2,4a,5-triaza-fluoren-1-one in 8 mL tetrahydrofuran, 30 μL (30 μg, 1.67 mmol) water, 0.16 mL (0.15 g, 2.11 mmol) cyclopropanecarboxaldehyde, 0.24 mL (0.25 g, 4.2 mmol) acetic acid and 2.1 mL (1.93 g, 2.1 mmol) sodium cyanoborohydride (1M solution in tetrahydrofuran) were added successively and the reaction mixture was stirred for 18 hours at 55° C. After cooling to room temperature the reaction was poured on 10% aqueous sodium bicarbonate solution and was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel with dichloromethane: methanol:ammonia (9:1:0.1 v/v) as eluant to give 0.19 g (40%) of the desired compound as a white solid.

後処理

  1. temperatureAfter cooling to room temperature the reaction
  2. extractionwas extracted three times with ethyl acetate
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was flash-chromatographed on silica gel with dichloromethane: methanol:ammonia (9:1:0.1 v/v) as eluant

出典と根拠

ORDレコード
ord-6bc3141338324e60a8a270f62cf5f39e
出典データセット
uspto-grants-2010_08
特許番号
US07786109B2

反応ノート

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