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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172314Generated: November 2, 2026

Acetic Acid → tert-butyl 4-(2-(1,2,3,4-tetrahydroisoquinolin-5-yl)-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/2172314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-butyl 4-(2-(isoquinolin-5-yl)-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 89813602—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
Producttert-butyl 4-(2-(1,2,3,4-tetrahydroisoquinolin-5-yl)-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 8981560183.1%

Reaction Steps

A solution of tert-butyl 4-(2-(isoquinolin-5-yl)-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate (9.80 g, 21.56 mmol) in 50 mL MeOH was treated with acetic acid (1.234 ml, 21.56 mmol) and platinum(IV) oxide (Sigma-Aldrich, St. Louis, Mo., 0.979 g, 4.31 mmol) and was placed under 45 psi (4559.6 kpa) H2 overnight. The reaction mixture was filtered through a plug of diatomaceous earth and concentrated. The resulting residue was taken up in DCM, was washed with saturated NaHCO3 solution, the organics dried over MgSO4 and concentrated yielding tert-butyl 4-(2-(1,2,3,4-tetrahydroisoquinolin-5-yl)-5-(trifluoromethyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate (8.21 g, 17.91 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051311B2
Source datasetuspto-grants-2015_06
ORD IDord-558e8924bbc843b5ac1e1c3d1ac6e06d
Source noteuspto-grants-2015_06