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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876467Generated: October 30, 2026

2-tert-Butyl-1,1,3,3-tetramethylguanidine → cis-Tert-butyl 4-fluoro-5-(2-(7-methyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yloxy)azepane-1-carboxylate

https://huagongshe.com/reaction/876467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
Reactanttrans-Tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylateHCID 131731013—
Reactant2-(7-Methyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-olHCID 136337810—
SolventAcetonitrileHCID 6342—
Productcis-Tert-butyl 4-fluoro-5-(2-(7-methyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yloxy)azepane-1-carboxylateHCID 131731017—

Reaction Conditions

Temperature40 °C

Reaction Steps

2-(7-methyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-ol (300 mg, 1.09 mmol) was suspended in CH3CN (5 mL) at ambient temperature, and trans-tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylate (454 mg, 1.09 mmol) and 2-tert-butyl-1,1,3,3-tetramethylguanidine (263 μL, 1.30 mmol) were added. The dark solution was stirred at 40° C. overnight, then concentrated to a grey solid which was slurried in water for 10 minutes. The solid was filtered, washed and dried in vacuo to provide the desired product. MS ESI (+) m/z 492.3 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987251B2
Source datasetuspto-grants-2015_03
ORD IDord-66679437cef240f1973853832b2971da
Source noteuspto-grants-2015_03