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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-tert-Butyl-1,1,3,3-tetramethylguanidine | HCID 3571581 | — |
| Reactant | trans-Tert-butyl 4-fluoro-5-(4-nitrophenylsulfonyloxy)azepane-1-carboxylate | HCID 131731013 | — |
| Reactant | 2-(7-Methyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-ol | HCID 136337810 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 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 | HCID 131731017 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987251B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-66679437cef240f1973853832b2971da |
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| Source note | uspto-grants-2015_03 |
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