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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108357Generated: October 31, 2026

Propargyl bromide → 1-[3-({4-Amino-7-[3-(1-piperidinyl)-1-propyn-1-yl]pyrrolo[2,1-f][1,2,4]triazin-5-yl}carbonyl)phenyl]-3-(2,4-dichlorophenyl)urea

https://huagongshe.com/reaction/2108357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPiperidineHCID 8082—
Reactant1-{3-[(4-Amino-7-bromopyrrolo[2,1-f][1,2,4]triazin-5-yl)carbonyl]phenyl}-3-(2,4-dichlorophenyl)ureaHCID 16739790—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Product1-[3-({4-Amino-7-[3-(1-piperidinyl)-1-propyn-1-yl]pyrrolo[2,1-f][1,2,4]triazin-5-yl}carbonyl)phenyl]-3-(2,4-dichlorophenyl)ureaHCID 5762946262%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of piperidine (2 mL) and propargyl bromide (80 wt % in toluene, 0.02 mL, 0.19 mmol) was purged with argon for 10 minutes. The solution was treated with 95G (20 mg, 0.04 mmol), CuI (1 mg, 0.008 mmol) and PdCl2(PPh3)2 (3 mg, 0.004 mmol). The reaction mixture was heated to 80° C. for one hour and then concentrated. The residue was purified by flash chromatography (SiO2, 0% to 10% MeOH/CH2Cl2) to afford the desired compound (13 mg, 62%). HPLC tR=3.17 min (Chromolith SpeedROD 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA, 4 min gradient, monitored at 254 nm). [M+H+]=562.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514435B2
Source datasetuspto-grants-2009_04
ORD IDord-f37761a994be495cbe329a85c46e07cd
Source noteuspto-grants-2009_04