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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180126Generated: October 31, 2026

Trifluoroacetic acid → HCID 10296729, compound

https://huagongshe.com/reaction/2180126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22490023HCID 22490023—
SolventDichloromethaneHCID 6344—
ProductHCID 10296729HCID 1029672962%

Reaction Steps

A solution of 7-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline (100 mg, 0.186 mmol) in methylene chloride (3 ml) containing TFA (1 ml) was stirred at ambient temperature for 2 hours. The volatiles were removed under vacuum. The residue was partitioned between water and methylene chloride and the pH of the aqueous layer was adjusted to 13 with 6N aqueous sodium hydroxide. The organic layer was separated, washed with water, brine, dried (MgSO4) and evaporated. The residue was triturated with ether/pentane (1/1). The solid was filtered, washed with pentane and dried under vacuum to give 4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxy-7-(piperidin-4-ylmethoxy)cinnoline (50 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887874B2
Source datasetuspto-grants-2005_05
ORD IDord-6512357a607b41b3a80792141612a370
Source noteuspto-grants-2005_05