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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926691Generated: November 3, 2026

Pyridine → HCID 57685257, compound

https://huagongshe.com/reaction/1926691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantN-Methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 57685258—
ReactantHCID 59346396HCID 59346396—
ProductHCID 57685257HCID 57685257—

Reaction Steps

To a solution of 3 (3.45 g, 8.2 mmol, 1.0 eq.),) and pyridine (0.66 ml, 0.82 mmol, 1.0 eq.),) in dichloromethane (40 ml) at 23° C. is added carbamoyl chloride 6 (3 g, 8.2 mmol, 1.0 eq.) drop wise over a period of 15 minutes. The reaction mixture is further stirred at room temperature for a period of 8 hours after which, it is partitioned between dichloromethane and water. The organic layer is separated and the aqueous layer is extracted with dichloromethane. The combined organic extracts are washed with water, dried over Na2SO4, filtered and concentrated to provide crude product 7. The residue is purified using column chromatography with MeOH/CH2Cl2 (5:1) as eluent to afford the title product 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183248B2
Source datasetuspto-grants-2012_05
ORD IDord-3c3a67b26afe484a9c91f4f97e685c16
Source noteuspto-grants-2012_05