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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | 7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 42281383 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-1,4-dioxaspiro[4.5]decan-8-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040691B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-69c7c35bce9e40b487c715e1a02256f4 |
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| Source note | uspto-grants-2015_05 |
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