تفاعل #170502

ord-b2ec02c3417d47ca87c35ad4e5ea6b0f

معادلة التفاعل

Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)O)cn1
6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acid
Cl.OC1CNC1
azetidin-3-ol hydrochloride
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
CCN(C(C)C)C(C)C
N-ethyldiisopropylamine
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CC(O)C2)cn1
title compound
المردود 91.0%
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CC(O)C2)cn1
(3-Hydroxy-azetidin-1-yl)-[6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridin-3-yl]-methanone
المردود 91.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting reaction mixture
  2. 2
    تركيزConcentration and purification by chromatography (SiO2, heptane:ethyl acetate=3:1 to 1:4)

الإجراء التجريبي

To a solution of 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acid (200 mg, 0.65 mmol) and azetidin-3-ol hydrochloride (70.7 mg, 0.65 mmol) in THF (6 mL) at 0° C. were added 1-hydroxybenzotriazole hydrate (100.8 mg, 0.65 mmol), N-ethyldiisopropylamine (281.7 μL, 1.613 mmol) and N-(3-dimethylaminopropy)-N′-ethylcarbodiimidazole hydrochloride (126.2 mg, 0.65 mmol). The resulting reaction mixture was stirred overnight at room temperature. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=3:1 to 1:4) afforded the title compound (215 mg, 91%) as a colourless oil. MS: m/e=366.2 [M+H]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846719B2uspto-grants-2014_09