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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204155Generated: October 31, 2026

Trifluoroacetic acid → HCID 58551369, compound

https://huagongshe.com/reaction/2204155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58551565HCID 58551565—
SolventDichloromethaneHCID 6344—
ProductHCID 58551369HCID 5855136999%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of tert-butyl 1′-methylsulfonylspiro[piperidine-4,4′-pyrrolo[2,1-c][1,4]benzoxazine]-1-carboxylate (200 mg, 0.48 mmol) in dry dichloromethane (1 mL) at 0° C. was added TFA (147 μL, 1.91 mmol). The cooling bath was removed and the mixture was stirred for 1.5 h at 25° C. The mixture was concentrated under reduced pressure and the residue obtained was taken up in dichloromethane (10 ml) and was washed with aqueous saturated NaHCO3 (5 ml). The aqueous phase was extracted twice with dichloromethane (2×10 ml) and the organic phases were combined, dried, filtered and concentrated to yield 1′-methylsulfonylspiro[piperidine-4,4′-pyrrolo[2,1-c][1,4]benzoxazine] as a light yellow foamy solid (150 mg, 99%). ESI-MS m/z calc. 318.1, found 319.3 (M+1)+; Retention time 0.93 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-90bd11962e29486394fc95b6f1ef36c5
Source noteuspto-grants-2016_06