Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972912Generated: October 31, 2026

Tetrahydrofuran → HCID 58529404, compound

https://huagongshe.com/reaction/1972912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
ReactantHCID 16066662HCID 16066662—
ProductHCID 58529404HCID 58529404—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-(2-benzyl-2H-indazol-6-yl)-7-piperidin-4-ylpyrrolo[2,1-f][1,2,4]triazin-4-amine (100 mg, 0.22 mmol) in THF (1.5 mL) was added (2-bromoethoxy)-tert-butyldimethylsilane (51 μL, 0.24 mmol) and N,N-diisopropylethylamine (114 μl, 0.65 mmol). The reaction was heated at 60° C. for 17 h and then cooled to rt. Additional (2-bromoethoxy)-tert-butyldimethylsilane (51 μL) and N,N-diisopropylethylamine (114 μl) were added and the mixture continued to stir at 60° C. for 64 h. The crude mixture was purified by preparative HPLC using a gradient elution from 20% to 50% acetonitrile in water followed by filtration through an acidic resin, washing with MeOH. The product was eluted with 2M NH3 in MeOH and the filtrate was concentrated. A solution of the residue in 1% HCl in 95:5 EtOH/H2O (4 mL) was stirred at rt for 16 h. The mixture was basified (pH 9) with the addition of saturated, aqueous NaHCO3 solution and was evaporated to remove volatiles. The aqueous mixture was extracted with ethyl acetate (3×15 mL) and the combined organic layers were washed with brine, dried (Na2SO4) and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-5d1abf05a10d4cf4ad2ea0992066531d
Source noteuspto-grants-2013_04