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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594159Generated: November 2, 2026

HCID 72194554, compound → HCID 72194553, compound

https://huagongshe.com/reaction/594159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 72194554HCID 72194554—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 72194553HCID 7219455373.6%

Reaction Steps

N-isobutyl-N-(3-methyl-5-(prop-1-en-2-yl)pyridin-2-yl)-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamide (83 mg, 0.18 mmol) was dissolved in ethyl acetate (3 mL) and methanol (3 mL). The reaction was hydrogenated using an H-cube flow hydrogenator (settings: room temperature, 1 bar, 1 mL/min flow rate) and a 10% Pd/C CatCart as the catalyst. Two clean fractions of product were collected along with a third impure fraction, the impure fraction was then purified by mass directed autoprep (formic acid modifier). The two clean product fractions and purified third fraction were then combined and evaporated to give the title compound (61 mg). LCMS (2 min, formic) Rt 1.45 min, m/z (ES+) 461 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242972B2
Source datasetuspto-grants-2016_01
ORD IDord-3fd71b69399b45b5910a349562488e63
Source noteuspto-grants-2016_01