Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166772Generated: November 1, 2026

Trifluoroacetic acid → HCID 73113646, compound

https://huagongshe.com/reaction/1166772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
Reactant3-Chloro-4-hydroxybenzohydrazideHCID 10954268—
ReactantHCID 22999110HCID 22999110—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 73113646HCID 73113646—

Reaction Steps

This compound was prepared analogously to the compound described in the previous example starting from resin bound 3-chloro-4-hydroxybenzoic acid hydrazide (resin—[building block 1]) (2 g, 2 mmoles), 4-(2-bromoethoxy)-3-chloro-5-methoxybenzaldehyde ([building block 2]) (0.81 g, 1.5 equivs.), and 1,2,3,4-tetrahydroisoquinoline ([building block 3]) (2.5 g, 10 equivs.). After cleavage with 50% trifluoroacetic acid, the residue (1.0 g) was dissolved in 15 ml of a mixture of 25% aq. ammonia, methanol and dichloromethane (1:9:90) and purified by column chromatography on silica gel (25 g) eluting with a mixture of methanol and dichloromethane (1:12). This afforded 0.11 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613942B1
Source datasetuspto-grants-2003_09
ORD IDord-b0940c8ddaf64fe1b7925103956344f2
Source noteuspto-grants-2003_09