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Cyclopentanone → (+/-)-3-Benzyl-2-(1-cyclopentylamino-propyl)-3H-pyrrolo[2,1-f][1,2,4]triazin-4-one

HRID 1795991
ノート
印刷プレビュー

反応式

HRID 1795991 の反応式
[NH2:1][CH:2]([C:5]1[N:10]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:9](=[O:18])[C:8]2=[CH:19][CH:20]=[CH:21][N:7]2[N:6]=1)[CH2:3][CH3:4].[C:22]1(=O)[CH2:26][CH2:25][CH2:24][CH2:23]1.C([O-])(=O)C.[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>O1CCOCC1>[CH2:11]([N:10]1[C:9](=[O:18])[C:8]2=[CH:19][CH:20]=[CH:21][N:7]2[N:6]=[C:5]1[CH:2]([NH:1][CH:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1)[CH2:3][CH3:4])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8452Cyclopentanone2 回HCID 517045Sodium AcetateHCID 5049666Sodium triacetoxyborohydride2 回HCID 221799762-(1-amino-propyl)-3-benzyl-3H-pyrrolo[2,1-f][1,2,4]triazin-4-one

生成物 1

HCID 22180088(+/-)-3-Benzyl-2-(1-cyclopentylamino-propyl)-3H-pyrrolo[2,1-f][1,2,4]triazin-4-one収率 71.3%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 2-(1-amino-propyl)-3-benzyl-3H-pyrrolo[2,1-f][1,2,4]triazin-4-one (Example 26, 50 mg, 0.16 mmol), cyclopentanone (13 mg, 0.16 mmol), anhydrous sodium acetate (26 mg, 0.32 mmol), 4 Å molecular sieves (50 mg) and 1,4-dioxane (10 mL) was stirred at room temperture for 40 min. The mixture was treated with sodium triacetoxyborohydride (51 mg, 0.24 mmol) in one portion and stirred at room temperature for 40 h. Additional portions of cyclopentanone (0.16 mmol) and sodium triacetoxyborohydride (0.16 mmol) were added to the mixture which was stirred for an additional 3.5 hours then filtered. The filtrate was partitioned between ethyl acetate and saturated sodium bicarbonate, the ethyl acetate phase washed with brine, dried (MgSO4) and concentrated. The residue was purified by flash column chromatography on silica gel eluting with ethyl acetate to give the title compound (40 mg, 71%): 1H NMR (DMSO-d6) δ 0.88 (t, 3H, J=7.15 Hz), 0.95 (m, 1H), 1.05 (m, 1H), 1.20 (m, 1H), 1.31 (m, 1H), 1.33 (m, 1H), 1.50–1.72 (m, 6H), 2.72 (m, 1H), 3.53 (m, 1H), 4.95 (m, 1H), 5.58 (m, 1H), 6.54 (s, 1H), 7.08 (s, 1H) 7.16 (s 2H), 7.24–7.35 (m, 3H), 7.35 (s, 1H).

後処理

  1. stirringstirred at room temperature for 40 h
  2. stirringwas stirred for an additional 3.5 hours
  3. filtrationthen filtered
  4. customThe filtrate was partitioned between ethyl acetate and saturated sodium bicarbonate
  5. washthe ethyl acetate phase washed with brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. customThe residue was purified by flash column chromatography on silica gel eluting with ethyl acetate

出典と根拠

ORDレコード
ord-1c4a5ba7bde74080b80ad17bd5554182
出典データセット
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07030118B2

反応ノート

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