تفاعل #2045069

ord-43499d775f7f45a9884f17e45398e0b0

معادلة التفاعل

Cc1ccc2c(N)ccc(O)c2n1
5-Amino-8-hydroxy-2-methylquinoline
[N-]=[N+]=[N-].[Na+]
sodium azide
O=N[O-].[Na+]
sodium nitrite
Cc1ccc2c(N=[N+]=[N-])ccc(O)c2n1
13
المردود 66.0%
Cc1ccc2c(N=[N+]=[N-])ccc(O)c2n1
5-Azido-8-hydroxy-2-methylquinoline
المردود 66.0%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
-3°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred for 20 min
  2. 2
    workup.STIRRINGstirred at 0° C. for a further 1.5 h
  3. 3
    درجة الحرارةto warm to room temperature over 24 h in the dark
  4. 4
    استخلاصIsolation by extraction with diethyl ether
  5. 5
    أخرىgave a dark brown solid, which
  6. 6
    أخرىwas recrystallized from light petroleum

الإجراء التجريبي

5-Amino-8-hydroxy-2-methylquinoline (12; 723 mg, 4.2 mmol) was dissolved in a solution of concentrated hydrochloric acid (0.4 mL) and water (5 mL), cooled to −3° C. in a salt-ice bath, stirred for 10 min, then treated dropwise with a cold solution of sodium nitrite (0.50 g, 7.2 mmol) in water (5 mL). The mixture was stirred for 20 min, then treated dropwise with sodium azide (0.60 g, 9.2 mmol) in water (40 mL), stirred at 0° C. for a further 1.5 h, then allowed to warm to room temperature over 24 h in the dark. Isolation by extraction with diethyl ether gave a dark brown solid, which was recrystallized from light petroleum to yield 13 as light brown crystals (554 mg, 66%). 1H NMR (500 MHz, CD3OD) δ ppm: 3.31 (s, 3H), 7.06 (d, J=8.5 Hz, 1H), 7.15 (d, J=8.5 Hz, 1H), 7.36 (d, J=8.5 Hz, 1H), 8.21 (d, J=8.5 Hz, 1H). 13C NMR (125 MHz, CD3OD) δ ppm: 24.9, 111.8, 115.6, 121.6, 123.7, 127.9, 132.6, 139.6, 151.1, 159.7. HRMS (ESI): calcd for C10H8N4O [M+H]+: 201.0771, found: 201.0773.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08409820B2uspto-grants-2013_04