تفاعل #1121778

ord-f6579016e68c42d0bf9d6ce82eae7f12

معادلة التفاعل

Nc1ncc(-c2ccccc2)nc1Br
2-amino-3-bromo-5-phenylpyrazine
Nc1ncc(-c2ccccc2)nc1Br
2-Amino-3-Bromo-5-phenylpyrazine
SC12CC3CC(CC(C3)C1)C2
1-adamantanethiol
[H-].[Na+]
sodium hydride
Nc1ncc(-c2ccccc2)nc1SC12CC3CC(CC(C3)C1)C2
title compound 18o
المردود 62.0%
Nc1ncc(-c2ccccc2)nc1SC12CC3CC(CC(C3)C1)C2
2-Amino-5-phenyl-3-adamantylthiopyrazine
المردود 62.0%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled
  2. 2
    أخرىquenched with water
  3. 3
    workup.ADDITIONThen EtOAc was added
  4. 4
    ترشيحfiltered
  5. 5
    أخرىthe solvent removed under reduced pressure
  6. 6
    أخرىto get a crude that
  7. 7
    أخرىwas purified by flash chromatography

الإجراء التجريبي

To a solution of 1-adamantanethiol (0.07 g, 0.4 mmol) in dry acetonitrile (10 mL), sodium hydride (NaH) (9 mg, 0.4 mmol) was added and the resulting mixture was stirred for 15 min. After this time 2-amino-3-bromo-5-phenylpyrazine 17b (0.05 g, 0.2 mmol) was added and the mixture heated at 80° C. for 4 h, cooled and quenched with water. Then EtOAc was added and the organic layer was anidrified over Na2SO4, filtered and the solvent removed under reduced pressure to get a crude that was purified by flash chromatography using petroleum ether-EtOAc (7:3 v/v) as eluent, to obtain 0.04 g of the title compound 18o as a yellow oil (62% yield). 1H-NMR (CDCl3): 1.73 (s, 6H), 2.08 (s, 3H), 2.23 (s, 6H), 5.13 (br s, 2H), 7.32-7.36 (m, 1H), 7.42-7.46 (m, 2H), 7.91-7.93 (m, 2H), 8.29 (s, 1H). MS (ESI): m/z 338 (M+H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546147B2uspto-grants-2013_10