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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273519Generated: October 31, 2026

Boron tribromide → 3-(3-amino-5-methyl-1,2,4-benzotriazin-7-yl)-4-chlorophenol

https://huagongshe.com/reaction/273519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant7-(2-Chloro-5-methoxyphenyl)-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822753—
SolventDichloromethaneHCID 6344—
Product3-(3-amino-5-methyl-1,2,4-benzotriazin-7-yl)-4-chlorophenolHCID 1150751073%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-(2-chloro-5-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-ylamine (0.158 g, 0.527 mmol, 1 equiv) was diluted with 10 mL DCM and chilled to 0° C. using an ice bath. A 1.0 M solution of BBr3 in DCM (3.16 mL, 3.16 mmol, 6.0 equiv) was then added in one portion resulting in a dark reaction mixture. The reaction was allowed to come to ambient temperature and stirred for 3.5 hours, then quenched by carefully pouring onto a saturated solution of sodium bicarbonate followed by sonication for 3-5 minutes. Additional DCM was added and this mixture was washed with sodium bicarbonate followed by brine. The organic phase was separated, dried over sodium sulfate (Na2SO4), filtered and evaporated to dryness. Solids were then diluted with minimum amount of ethyl acetate and precipitated out with hexanes. Product was filtered off and dried to yield a yellow solid (0.110 g, 73% yield). MS (ESI+): m/z 287.1, LC retention time: 2.46 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456176B2
Source datasetuspto-grants-2008_11
ORD IDord-f410e96d1e754621a511c6059546ae66
Source noteuspto-grants-2008_11