Réaction #339170

ord-f1190df80bd74866b15f1d129ebc4b42

Équation de réaction

Cc1cc(Cl)cc(C(=O)O)c1N
2-amino-5-chloro-3-methylbenzoic acid
N#Cc1cccnc1-n1cc(Br)cc1C(=O)O
4-bromo-1-(3-cyano-2-pyridinyl)-1H-pyrrole-2-carboxylic acid
Nc1c(Br)cc(Br)cc1C(=O)O
2-amino-3,5-dibromobenzoic acid
O=C(O)c1cc(Br)cn1-c1ncccc1Cl
4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid
N#Cc1cccnc1-n1cc(Br)cc1-c1nc2c(Br)cc(Br)cc2c(=O)o1
6,8-dibromo-2-[4-bromo-1-(3-cyano-2-pyridinyl)-1H-pyrrol-2-yl]-4H-3,1-benzoxazine-4-one

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

According to the same manner as that of Reference Preparation Example 71-(5), 4-bromo-1-(3-cyano-2-pyridinyl)-1H-pyrrole-2-carboxylic acid and 2-amino-3,5-dibromobenzoic acid were used in place of 4-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrrole-2-carboxylic acid and 2-amino-5-chloro-3-methylbenzoic acid respectively to obtain 6,8-dibromo-2-[4-bromo-1-(3-cyano-2-pyridinyl)-1H-pyrrol-2-yl]-4H-3,1-benzoxazine-4-one of the formula:

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07867949B2uspto-grants-2011_01