反応 #44791

ord-12f3c925492145d0a0794d5e263a0a0a

反応方程式

O=C([O-])O
bicarbonate
c1ccc(COc2ccc(CN3CCCNCC3)cc2)cc1
hexahydro-1-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine
COC(=O)CCBr
methyl 3-bromopropanoate
CCN(CC)CC
triethylamine
COC(=O)CCN1CCCN(Cc2ccc(OCc3ccccc3)cc2)CC1
methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-propanoate
収率 51.7%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the reaction was heated
  2. 2
    温度at reflux for 4 hours
  3. 3
    温度to cool
  4. 4
    洗浄The combined ethyl acetate extracts were washed with water
  5. 5
    その他dried
  6. 6
    濃縮concentrated

実験手順

A solution of hexahydro-1-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine (150 mg, 0.506 mmol) and methyl 3-bromopropanoate (0.22 mL, 2.0 mmol) in THF (6 mL) was treated with triethylamine (0.28 mL, 2 mmol) and the reaction was heated at reflux for 4 hours. The reaction was allowed to cool and treated with an aqueous bicarbonate solution. The combined ethyl acetate extracts were washed with water, dried and concentrated to give 0.1 g of methyl hexahydro-4-[[4-(phenylmethoxy)phenyl]methyl]-1H-1,4-diazepine-1-propanoate; 1H NMR (300 MHz, CDCl3) δ 7.44 (d, 2H), 7.39 (dd, 2H), 7.32 (dd, 1H), 7.24 (d, 2H), 6.93 (d, 2H), 5.05 (s, 2H), 3.67 (s, 3H), 3.56 (s, 2H), 2.85 (t, 2H), 2.48 (t, 2H), 2.77-2.58 (m, 8H), 1.77 (m, 2H) ppm.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07737145B2uspto-grants-2010_06