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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090483Generated: November 4, 2026

HCID 59402271, compound → HCID 59402254, compound

https://huagongshe.com/reaction/2090483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59402271HCID 59402271—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59402254HCID 59402254—

Reaction Steps

To a solution of tert-butyl 4-{2-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3-methyl-1,2,3,4-tetrahydroisoquinolin-7-yl}-3,6-dihydropyridine-1(2H)-carboxylate (Example 43, Step 1) (0.20 g, 0.38 mmol) in methanol (5 mL) was added palladium on carbon 10% wt. (20 mg) under an atmosphere of nitrogen. The mixture was vacuumed and re-charged with hydrogen three times, and stirred at r.t. for 48 h. The mixture was filtered. The filtrate was concentrated to afford the desired product which was directly used in next step reaction without further purification (200 mg, 99.61%). LCMS (M+H)+: m/z=522.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436008B2
Source datasetuspto-grants-2013_05
ORD IDord-37deef81a05e448696c9236bfd7ff743
Source noteuspto-grants-2013_05