تفاعل #56970

ord-9f52a0b237554671b007a66dc5a2d955

معادلة التفاعل

NC1CCCc2c1[nH]c1ccc(Br)cc21
6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine
COc1cccc(C(=O)Cl)c1
m-anisoyl chloride
COc1cccc(C(=O)NC2CCCc3c2[nH]c2ccc(Br)cc32)c1
N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-3-methoxybenzamide

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-3-methoxybenzamide was prepared from 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine and m-anisoyl chloride in a similar manner as described above to give an orange solid (49% yield). 1H-NMR (CDCl3): δ 8.92 (s, 1H), 7.61 (m, 1H), 7.38-7.30 (m, 2H), 7.30-7.25 (m, 1H), 7.23 (m, 1H), 7.17 (d, 1H), 7.08-7.02 (m, 1H), 6.39 (d, 1H), 5.32 (m, 1H), 3.85 (s, 3H), 2.72 (m, 2H), 2.31 (m, 1H), 1.97 (m, 3H); MS m/z 399 (M−1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07419997B2uspto-grants-2008_09