반응 #167215

ord-268c04b1e14c42b48aaeb2e69afaef06

반응 방정식

O=C1NCCCN1c1cccnc1
1-pyridin-3-yl-tetrahydro-pyrimidin-2-one
Brc1ccc2ccccc2c1
2-bromo-naphthalene
N[C@@H]1CCCC[C@H]1N
trans-1,2-diamino cyclohexane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C1N(c2cccnc2)CCCN1c1ccc2ccccc2c1
product
수율 35.7%
O=C1N(c2cccnc2)CCCN1c1ccc2ccccc2c1
1-Naphthalen-2-yl-3-pyridin-3-yl-tetrahydro-pyrimidin-2-one
수율 35.7%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to afford the crude product
  2. 2
    기타Purification by column chromatography on silica gel (1% MeOH in chloroform)

실험 절차

Using the same reaction conditions as in Example 1, 1-pyridin-3-yl-tetrahydro-pyrimidin-2-one (I-10b: 118 mg, 0.724 mmol) was reacted with 2-bromo-naphthalene (150 mg, 0.724 mmol), 1,4-dioxane (5 mL), copper iodide (13.79 mg, 0.0724 mmol), trans-1,2-diamino cyclohexane (24.865 mg, 0.2172 mmol) and potassium carbonate (200 mg, 1.448 mmol) to afford the crude product. Purification by column chromatography on silica gel (1% MeOH in chloroform) afforded 75 mg of the product (35.71% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045173E1uspto-grants-2014_09