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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035694Generated: October 30, 2026

tert-Butyl 4-ethynylpiperidine-1-carboxylate → tert-Butyl 4-{1-[6-fluoro-2-oxo-1-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl]-1H-1,2,3-triazol-4-yl}piperidine-1-carboxylate

https://huagongshe.com/reaction/2035694

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-ethynylpiperidine-1-carboxylateHCID 15550481—
Reactant3-azido-6-fluoro-1-(2,2,2-trifluoroethyl)-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 58063523—
Producttert-Butyl 4-{1-[6-fluoro-2-oxo-1-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl]-1H-1,2,3-triazol-4-yl}piperidine-1-carboxylateHCID 66683843—

Reaction Steps

tert-Butyl 4-{1-[6-fluoro-2-oxo-1-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl]-1H-1,2,3-triazol-4-yl}piperidine-1-carboxylate was prepared from tert-butyl 4-ethynylpiperidine-1-carboxylate (synthesized from tert-butyl 4-formylpiperidine-1-carboxylate and Bestmann's reagent under standard condition) and 3-azido-6-fluoro-1-(2,2,2-trifluoroethyl)-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one under standard click chemistry condition. MS calculated 512.2 (MH+), exp 521.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575150B2
Source datasetuspto-grants-2013_11
ORD IDord-c075260d374848c5954136ed819ec749
Source noteuspto-grants-2013_11