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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639534Generated: November 2, 2026

Trifluoroacetic acid → HCID 66722795, compound

https://huagongshe.com/reaction/1639534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMorpholineHCID 8083—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantBenzoic acid, 3-(aminocarbonyl)-4-hydroxy-, methyl esterHCID 10607886—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 66722795HCID 6672279539.1%

Reaction Steps

A mixture of 125 mg (0.64 mmol) of methyl 3-carbamoyl-4-hydroxybenzoate, 192 mg (0.96 mmol) of 1-Boc-4-piperidone, and 120 μL of morpholine in 10 mL of MeOH is refluxed for 72 hr. The MeOH is removed by rotoevapoation, and DCM is added to the residue. Insoluble material is filtered off, and the filtrate is concentrated by rotoevaporation. The residue is purified by preparative TLC to give 93 mg (0.25 mmol, 39% yield) of 1′-(tert-butyloxycarbonyl)-6-methoxycarbonylspiro[1,3-benzoxazine-2,4′-piperidine]-4(3H)-one which on treatment with 40% TFA in dichloromethane gives the TFA salt of 6-methoxycarbonylspiro[1,3-benzoxazine-2,4′-piperidine]-4(3H)-one in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110570B2
Source datasetuspto-grants-2012_02
ORD IDord-069857009ea74cb1a94fa9db8f392fbb
Source noteuspto-grants-2012_02