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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615468Generated: October 31, 2026

tert-butyl 4-(4-amino-6-(3-(pyrrolidin-1-yl)propyl)pyrrolo[2,1-f][1,2,4]triazin-7-yl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(4-amino-6-(3-(pyrrolidin-1-yl)propyl)pyrrolo[2,1-f][1,2,4]triazin-7-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1615468

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(4-amino-6-(3-(pyrrolidin-1-yl)propyl)pyrrolo[2,1-f][1,2,4]triazin-7-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 66601711—
CatalystAdams' catalystHCID 345198—
SolventAcetateHCID 175—
ProductTert-butyl 4-(4-amino-6-(3-(pyrrolidin-1-yl)propyl)pyrrolo[2,1-f][1,2,4]triazin-7-yl)piperidine-1-carboxylateHCID 66614420100.1%

Reaction Steps

In a pressure reactor (50 mL), a mixture of the compound (132 mg, 0.31 mmol) prepared in Example 17 and platinum (IV) oxide in acetyl hydroxide (10 mL) was stirred under hydrogen atmosphere (3 atm). At 6 hours, the mixture was filtered through celite, eluting with acetyl hydroxide. The solvent was removed in vacuo. The resulting material extracted with DCM/sodium bicarbonate aqueous solution. The organic layers were dried over sodium sulfate, filtered and the solvent removed in vacuum to obtain the title compound (133 mg) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765754B2
Source datasetuspto-grants-2014_07
ORD IDord-0e9a2bccad184a8e878e419f8f6f8ad1
Source noteuspto-grants-2014_07