反応 #1869181

ord-8edc50dcb802428d8fb2902680b5c810

反応方程式

O=C1c2ccccc2OC2(CCNCC2)CN1Cc1ccccc1
compound
O=C1c2ccccc2OC2(CCNCC2)CN1Cc1ccccc1
4-benzyl-3,4-dihydro-5H-spiro[1,4-benzoxazepine-2,4′-piperidin]-5-one
O=CCCc1ccccc1
3-phenylpropanal
O=C1c2ccccc2OC2(CCN(CCCc3ccccc3)CC2)CN1Cc1ccccc1
4-benzyl-1′-(3-phenylpropyl)-3,4-dihydro-5H-spiro[1,4-benzoxazepine-2,4′-piperidin]-5-one

反応条件

温度
25°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter stirring overnight
  2. 2
    ろ過the mixture was filtered
  3. 3
    濃縮the filtrate was concentrated
  4. 4
    その他to give the compound of the present invention

実験手順

To a solution of the compound prepared in Example 30 (0.01 mmol) in tetrahydrofuran (0.4 mL) were added 3-phenylpropanal (0.02 mmol) and MP-BH(OAc)3 (Argonaut, product number 800415, loading; 2.25 mmol/g) (13.3 mg). The mixture was stirred overnight at 25° C. To the reaction mixture were added tetrahydrofuran (0.4 mL) and PS-NHNH2 (Argonaut, product number 800272, loading; 3.65 mmol/g) (8.2 mg). After stirring overnight, the mixture was filtered and the filtrate was concentrated to give the compound of the present invention having the following physical data.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07498323B2uspto-grants-2009_03