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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425752Generated: October 27, 2026

Methanol → HCID 86761341, compound

https://huagongshe.com/reaction/2425752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
ReactantHCID 59822470HCID 59822470—
ProductHCID 86761341HCID 8676134145%

Reaction Steps

A solution of 1-isopropyl-5-methyl-2-oxo-N-(piperidin-4-ylmethyl)-1,2-dihydroquinoline-3-carboxamide (150 mg, 0.44 mmol, step 4 in preparation 3) and tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (112 mg, 0.53 mmol, Castro Jose L. et al., J. Med. Chem., 1998, 41, 2667) in methanol (5 mL) was heated at 80° C. overnight. After cooled to room temperature, concentrated gave yellow oil. The residue was chromatographed on a column of silica gel eluting with 25% ammonium hydroxide/methanol/dichloromethane (2/10/100) to give 111 mg (45%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-fb44c75cc00d4a618ebd8a9d70bbf593
Source noteuspto-grants-2011_06