تفاعل #2328986

ord-f78d0bd165cd4cf9825f747c0d83e1fb

معادلة التفاعل

COc1ccc2nc(-c3ccc(N(C)C)nc3)oc2c1
5-(6-Methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine
Br
hydrogen bromide
O=C([O-])O.[Na+]
sodium bicarbonate
CN(C)c1ccc(-c2nc3ccc(O)cc3o2)cn1
title compound
المردود 19.6%
CN(C)c1ccc(-c2nc3ccc(O)cc3o2)cn1
2-[6-(Dimethylamino)pyridin-3-yl]-1,3-benzoxazol-6-ol
المردود 19.6%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe solid was collected
  2. 2
    workup.DISSOLUTIONThe solid was then dissolved in CH2Cl2/ethyl acetate
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    ترشيحfiltered
  5. 5
    أخرىevaporated in vacuo

الإجراء التجريبي

5-(6-Methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine (31 mg, 0.12 mmol) was mixed with hydrogen bromide (48% aq., 2 mL) and a crystal of tetrabutylammonium bromide was added. The reaction was run at 120° C. for 5 minutes in a microwave reactor. The reaction mixture was added to sodium bicarbonate (sat. aq.) and the solid was collected. The solid was then dissolved in CH2Cl2/ethyl acetate, dried (MgSO4), filtered and evaporated in vacuo, giving the title compound (6 mg) as a purple solid. 1H NMR (400 MHz, CD3OD) δ ppm 8.83 (d, 1H) 8.17 (dd, 1H) 7.44 (d, 1H) 7.02 (d, 1H) 6.75-6.88 (m, 2H) 3.19 (s, 6H); MS m/z (M+H) 256; (M−H) 254.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07670591B2uspto-grants-2010_03