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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712675Generated: October 31, 2026

HCID 123135825, compound → HCID 117667711, compound

https://huagongshe.com/reaction/712675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 123135825HCID 123135825—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 117667711HCID 11766771170.4%

Reaction Steps

5% Pd on carbon (150 mg, 0.07 mmol) is added to a solution of 6-[5-(-3-methanesulfonyl-propenyl)-pyridin-3-yl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester (340 mg, 0.79 mmol) in MeOH (30 mL). The mixture is stirred at room temperature under H2 atmosphere of 40 PSI for 16 hrs. After filtration, the filtrate is concentrated to give 240 mg of 6-[5-(3-methanesulfonyl-propyl)-pyridin-3-yl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester. This is then used to prepare 6-[5-(3-methanesulfonyl-propyl)-pyridin-3-yl]-1,2,3,4-tetrahydro-[1,8]naphthyridine according to the procedure for Step 2 of Example 27 using 20% trifluoroacetic acid in DCM as the reagent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-0d26dc422a8d4d7c85158e2ffd9517a3
Source noteuspto-grants-2015_11