Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117129Generated: October 29, 2026

N-bromobutanimide → 5-(Bromomethyl)-4-chloropyrrolo[2,1-f][1,2,4]triazine

https://huagongshe.com/reaction/2117129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Chloro-5-methylpyrrolo(2,1-f)(1,2,4)triazineHCID 21874227—
SolventCarbon TetrachlorideHCID 5943—
Product5-(Bromomethyl)-4-chloropyrrolo[2,1-f][1,2,4]triazineHCID 2187438692%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloro-5-methyl-pyrrolo[2,1-f][1,2,4]triazine (2.0 g, 11.93 mmol, WO 03/042172) and AKIN (195 mg, 1.19 mmol) in CCl4 (80 mL) under N2 was heated to 100° C. for 5 min, NBS (2.55 g, 14.3 mmol) was added. The reaction mixture was stirred for 10 min, then cooled to rt, filtered. The CCl4 layer was washed with dilute NaHCO3 aqueous solution, dried (MgSO4), filtered and concentrated to give the desired product (2.70 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439246B2
Source datasetuspto-grants-2008_10
ORD IDord-bbbe905d422f4b62bebbfbf6a0bb124f
Source noteuspto-grants-2008_10