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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256982Generated: October 25, 2026

4-Bromo-5-fluoro-2-methylaniline → 5-Bromo-4-fluoro-7-methyl-1h-benzotriazole

https://huagongshe.com/reaction/1256982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-5-fluoro-2-methylanilineHCID 7018044—
Reactant4-Bromo-3-fluoro-6-methyl-2-nitroanilineHCID 87077956—
Reactant5-Bromo-4-fluoro-7-methyl-1h-benzotriazoleHCID 178422453—
Product2-amino-3-(5-bromo-4-fluoro-7-methyl-2H-benzotriazol-2-yl)-2-methylpropionitrileHCID 66620468—
Product4-Bromo-3-fluoro-6-methyl-2-nitroanilineHCID 87077956—
Product5-Bromo-4-fluoro-7-methyl-1h-benzotriazoleHCID 17842245385%

Reaction Steps

2-Amino-3-(5-bromo-4-fluoro-7-methyl-2H-benzotriazol-2-yl)-2-methylpropionitrile [1.3 g, Rf=0.2 (1:1 EA/heptane)] was prepared using a procedure similar to that described in Example 1, part a and b, except starting from 5-bromo-4-fluoro-7-methyl-1H-benzotriazole. 5-Bromo-4-fluoro-7-methyl-1H-benzotriazole (4 g, 85%) was prepared using a procedure similar to that described in Example 11, part a, except starting from 4-bromo-3-fluoro-6-methyl-2-nitroaniline. 4-Bromo-3-fluoro-6-methyl-2-nitroaniline (6.1 g) was prepared using a procedure similar to that described in Example 39, part a, b and c, except starting from 4-bromo-5-fluoro-2-methylaniline (10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461176B2
Source datasetuspto-grants-2013_06
ORD IDord-ce92723f892a47f3acc12e66cb017438
Source noteuspto-grants-2013_06