Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122046Generated: November 2, 2026

Pyridine → HCID 68901099, compound

https://huagongshe.com/reaction/2122046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantN-Methyl-N-[(3S,4S)-4-methyl-3-piperidyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 12084830—
SolventDichloromethaneHCID 6344—
ProductHCID 68901099HCID 6890109932%

Reaction Steps

To a stirred solution of 1 mL of pyridine and 9 ml of dichloromethane was added 40 mg (0.163 mmol) of the product from Method H and 20 L of 4-methoxy-benzenesulfonyl chloride and the resulting mixture stirred at room temperature for 18 hours. The reaction was then quenched upon addition of saturated NaHCO3 (aq), the organic layer was removed and the aqueous layer extracted with dichloromethane. The dichloromethane layer was dried over Na2SO4 and concentrated to dryness in vacuo. The residue was purified by PTLC (silica; 10:1 dichloromethane/methanol) affording 22 mg (32%) of the title compound as a light yellow solid. LRMS: 416.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696567B2
Source datasetuspto-grants-2004_02
ORD IDord-484f3b143e964aa297ff672887914538
Source noteuspto-grants-2004_02