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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578754Generated: October 26, 2026

Chlorotrimethylsilane → 8-(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/578754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Reactant7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 42281383—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product8-(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 90389149—

Reaction Steps

7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine (9.20 g, 35.41 mmol) was dissolved in THF (105 mL) under argon at room temperature. Chlorotrimethylsilane (9.08 mL, 7.77 g, 70.82 mmol, 2 eq.) was added, and the mixture was stirred at room temperature for 3 h. It was then cooled to 0° C., and 2-propyl magnesium chloride (74 mL of a 2.0 M solution in THF, 149 mmol, 4.2 eq.) was added. The mixture was stirred for further 3 h while warming up to room temperature. Then, 1,4-dioxaspiro[4.5]decan-8-one (8.38 g, 53.12 mmol, 1.5 eq.) was added, and stirring was continued for another 16 h. The reaction was quenched with a 1:1 mixture of concentrated aqueous ammonium chloride solution and ice until the pH value reached 6-7. The mixture was extracted with two portions of ethyl acetate, and the combined organic extracts were dried over anhydrous sodium carbonate and concentrated to dryness. The title compound was crystallized from diethyl ether. Yield: 6.05 g (58% of th.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040691B2
Source datasetuspto-grants-2015_05
ORD IDord-69c7c35bce9e40b487c715e1a02256f4
Source noteuspto-grants-2015_05