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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582136Generated: October 31, 2026

Tetrahydrofuran → HCID 86588844, compound

https://huagongshe.com/reaction/1582136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant4-{2-[(2-chloro-6-methoxy-pyridine-4-carbonyl)-amino]-4-methoxy-benzothiazol-7-yl}-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl esterHCID 86588845—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86588844HCID 8658884430.2%

Reaction Steps

To a solution of 0.39 g (0.73 mMol) of 4-{2-[(2-chloro-6-methoxy-pyridine-4-carbonyl)-amino]-4-methoxy-benzothiazol-7-yl}-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester in 16.0 ml of methanol and 16.0 ml THF 100 mg of Pd/C (10%) and 0.15 ml triethyl amine were added. The reaction mixture was hydrogenated at 60° C. for 6 h, then filtered and evaporated to dryness in vacuo. The residue was subjected to column chromatography (ethyl acetate/hexane 1:1) to yield 0.110 g (30%) 4-{4-methoxy-2-[(2-methoxy-pyridine-4-carbonyl)-amino]-benzothiazol-7-yl}-piperidine-1-carboxylic acid tert-butyl ester as a white foam. ES-MS m/e (%): 499 ([M+H]+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734179B2
Source datasetuspto-grants-2004_05
ORD IDord-a293a2555d6847cfb9346d2687aa4a50
Source noteuspto-grants-2004_05