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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644520Generated: November 1, 2026

Trifluoroacetic acid → HCID 66775076, compound

https://huagongshe.com/reaction/1644520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86642667HCID 86642667—
SolventDichloromethaneHCID 6344—
ProductHCID 66775076HCID 66775076105.4%

Reaction Steps

A solution of tert-butyl{1-[2-(7-methoxy-2-oxoquinoxalin-1(2H)-yl)propyl]piperidin-4-yl}carbamate (Intermediate 222, 200 mg, 0.48 mmol) in dichloromethane (30 mL) was treated with trifluoroacetic acid (3 mL). After 2 hours, the reaction was concentrated to dryness. The residue was partitioned between 15% methanol/chloroform. The aqueous phase was re-extracted 3× with 15% methanol/chloroform. The combined organic phases were dried over magnesium sulfate, filtered, and concentrated to dryness giving 160 mg (100%) of the crude product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124602B2
Source datasetuspto-grants-2012_02
ORD IDord-9b4c7e5c22c540668f98143efcc04dfb
Source noteuspto-grants-2012_02