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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695798Generated: November 2, 2026

Pyridine → HCID 44539936, compound

https://huagongshe.com/reaction/1695798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Methyl-1,3-thiazole-4-carbonyl chlorideHCID 21183959—
ReactantHCID 58255824HCID 58255824—
SolventDichloromethaneHCID 6344—
ProductHCID 44539936HCID 4453993618.6%

Reaction Steps

N-{5-[4-Amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-3-pyridinyl}methanesulfonamide (50 mg) was dissolved in DCM (1 ml) and pyridine (0.014 ml) was added. A solution of 2-methyl-1,3-thiazole-4-carbonyl chloride (22 mg) in DCM (1 ml) was added to the reaction and the mixture was stirred at RT for 30 min. Further 2-methyl-1,3-thiazole-4-carbonyl chloride (10 mg) was added to the reaction and stirring continued for 30 min. Further 2-methyl-1,3-thiazole-4-carbonyl chloride (40 mg) was added then the reaction was quenched with water and passed through a hydrophobic frit. The organic layer was evaporated to dryness and the residue was dissolved in DMSO:MeOH (1 ml, 1:1, v/v) and purified by MDAP (method E). The compound was dissolved in MeOH containing a few drops of 2M NaOH and stirred for 5 mins at RT. The residue was dissolved in MeOH and loaded onto an SAX SPE cartridge pre-conditioned with MeOH. After eluting with MeOH and evaporating to dryness, the residue was dissolved in DMSO and purified by MDAP (method E) to give the title compound (9 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163743B2
Source datasetuspto-grants-2012_04
ORD IDord-c7cb0f6b7c474da2a7c1ab2f6f2a141d
Source noteuspto-grants-2012_04