반응 #8470

ord-e9297e9f797943d9b05989f796ddd673

반응 방정식

O=C(O)CCN1CCCCC1
1-piperidinepropionic acid
CCN=C=NCCCN(C)C.Cl
WSC.HCl
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
Cc1cccn2cc(-c3ccc(N)cc3)nc12
product
Cc1cccn2cc(-c3ccc(N)cc3)nc12
2-(4′-aminophenyl)-8-methylimidazo[1,2-a]pyridine
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
Cc1cccn2cc(-c3ccc(NC(=O)CCN4CCCCC4)cc3)nc12
title compound
수율 23.9%
Cc1cccn2cc(-c3ccc(NC(=O)CCN4CCCCC4)cc3)nc12
2-[4′-[3-(Piperidinyl)]propanamidophenyl]-8-methylimidazo[1,2-a]pyridine
수율 23.9%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThe mixture was poured into a separatory funnel
  2. 2
    세척washed sequentially with an equal volume of 1 N sodium hydroxide and water
  3. 3
    건조The organic phase was dried over sodium sulfate
  4. 4
    기타decanted
  5. 5
    기타evaporated
  6. 6
    기타The residue was purified via silica gel chromatography (methanol/dichloromethane)

실험 절차

To a mixture of the product of Step B (330 mg) and N,N-diisopropylethylamine (0.28 mL) in dichloromethane (3 mL) and N,N-dimethylformamide (1 mL), was added 1-piperidinepropionic acid (256 mg), WSC.HCl (1-Ethyl-3-(3′dimethylaminopropyl)-carbodiimide.HCl) (312 mg), and 1-hydroxybenzotriazole hydrate (220 mg). The solution was stirred at ambient temperature for approximately 18 hours. The mixture was poured into a separatory funnel and washed sequentially with an equal volume of 1 N sodium hydroxide and water. The organic phase was dried over sodium sulfate, decanted and evaporated. The residue was purified via silica gel chromatography (methanol/dichloromethane) to yield the title compound (128 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087757B2uspto-grants-2006_08