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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422695Generated: November 3, 2026

Trifluoroacetic acid → HCID 178487965, compound

https://huagongshe.com/reaction/1422695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178487967HCID 178487967—
SolventDichloromethaneHCID 6344—
ProductHCID 178487965HCID 17848796595%

Reaction Steps

Trifluoroacetic acid (6.33 mL, 82.2 mmol, 20 eq) is added at room temperature to a stirred solution of {trans-4-[2-(6-methoxy-[1,5]naphthyridin-3-yloxy)-ethyl]-cyclohexyl}-carbamic acid tort-butyl ester (1.65 g, 4.11 mmol, 1.0 eq) in dichloromethane (100 mL). After 2 hours stirring at room temperature, the reaction mixture is partitioned between saturated sodium hydrogen carbonate aqueous solution and dichloromethane and the pH value is about 10. The combined organic layers are dried over sodium sulfate and concentrated to afford trans-4-[2-(6-methoxy-[1,5]naphthyridin-3-yloxy)-ethyl]-cyclohexylamine as a yellow solid (1.24 g, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927542B2
Source datasetuspto-grants-2015_01
ORD IDord-d9215bfa12284db68a659efb91c882de
Source noteuspto-grants-2015_01