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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987133Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → HCID 16035853, compound

https://huagongshe.com/reaction/1987133

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 57722777HCID 57722777—
SolventMethanolHCID 887—
ProductHCID 16035853HCID 16035853—

Reaction Steps

3-chloro-7-oxiran-2-yl-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (60 mg, 0.21 mmol) was suspended in 2.5 mL of methanol. tert-Butyl piperazine-1-carboxylate (98 mg, 0.53 mmol) was added and the reaction was heated to reflux for 8 hours. The resulting mixture was concentrated in vacuo and purified directly via flash chromatography (15-100% ethyl acetate/hexanes) to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 9.79 (d, 1H); 8.49 (d, 1H); 8.22 (d, 1H); 7.77 (dd, 1H); 7.60 (d, 1H); 7.31 (d, 1H); 7.25 (d, 1H); 4.91 (dd, 1H); 3.50-3.45 (m, 4H); 2.72 (broad s, 2H); 2.63 (dd, 1H); 2.50 (dd, 1H); 2.44 (broad s, 2H); 1.46 (s, 9H). Hydroxyl proton was not observed. LRMS (APCI) calc'd for (C25H29ClN3O4) [M+H]+, 470.2; found 470.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550478B2
Source datasetuspto-grants-2009_06
ORD IDord-0749746c4a6e4a9784b121efeb208487
Source noteuspto-grants-2009_06