Butylamine → HCID 9901307, compound

HRID 1829752Notes

Reaction equation

HRID 1829752 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([CH2:12][OH:13])=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1.[CH2:15]([NH2:19])[CH2:16][CH2:17][CH3:18]>N1CCCC1>[CH2:15]([NH:19][C:12]([C:8]1[CH:7]=[C:6]2[C:11]([C:2]([N:19]3[CH2:18][CH2:17][CH2:16][CH2:15]3)=[CH:3][C:4]([CH3:14])=[N:5]2)=[CH:10][CH:9]=1)=[O:13])[CH2:16][CH2:17][CH3:18]

Participants

4

Reactant 2

HCID 8007ButylamineHCID 11264243HCID 11264243, compound

Product 1

HCID 9901307HCID 9901307, compoundYield 43%

Reagents, catalysts & solvents 1

HCID 31268PyrrolidineSolvent

Procedure

(4-Chloro-2-methyl-quinolin-7-yl)-methanol (example 2, 200 mg, 0.80 mmol) was refluxed in butylamine (2 mL) for 6 h. After cooling the reaction mixture was partitioned between sat. aq. ammonium chloride solution and dichloromethane. The organic layer was separated, dried (MgSO4), and evaporated. The residue was chromatographed (SiO2, CH2Cl2/MeOH 19:1) to produce a yellow oil, which was heated in pyrrolidine (2 mL) at 70° C. for 16 h. After cooling the reaction mixture was partitioned between sat. aq. ammonium chloride solution and dichloromethane. The organic layer was separated, dried (MgSO4), and evaporated. Chromatography (SiO2, dichloromethane/methanol 19:1) afforded the title compound (108 mg, 43%). White solid, ISP-MS: m/e=312.3 ([M+H]+).

Workup

  1. temperatureAfter cooling the reaction mixture
  2. customwas partitioned between sat. aq. ammonium chloride solution and dichloromethane
  3. customThe organic layer was separated
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customThe residue was chromatographed (SiO2, CH2Cl2/MeOH 19:1)
  7. customto produce a yellow oil, which
  8. temperatureAfter cooling the reaction mixture
  9. customwas partitioned between sat. aq. ammonium chloride solution and dichloromethane
  10. customThe organic layer was separated
  11. dry with materialdried (MgSO4)
  12. customevaporated

Sources & evidence

ORD record
ord-21595563b10443b9b8f09276c1f8b7a0
Source dataset
uspto-grants-2006_06
Patent number
US07064134B2

Reaction notes

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