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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188110Generated: November 3, 2026

HCID 59408769, compound → HCID 25001105, compound

https://huagongshe.com/reaction/1188110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59408769HCID 59408769—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25001105HCID 25001105119.6%

Reaction Steps

BMS was added to a solution of 2-(benzylamino)-N-(5-(4-fluorophenyl)-1H-pyrazol-3-yl)thiazole-5-carboxamide (50 mg, 0.13 mmol) in THF (1 mL). The resulting solution was stirred at RT overnight. The reaction was then quenched with MeOH (0.5 mL) and 1N HCl was added until pH=2. After stirring the reaction mixture at RT for 3 hrs, the organic solvents were evaporated and the aqueous solution was neutralized with a NaHCO3 saturated aqueous solution, extracted with AcOEt, dried with Na2SO4 and concentrated. The crude product was purified by column (0-2% MeOH/AcOEt gradient), yielding N-benzyl-5-((5-(4-fluorophenyl)-1H-pyrazol-3-ylamino)methyl)thiazol-2-amine (59 mg, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673940B2
Source datasetuspto-grants-2014_03
ORD IDord-e556e6de88864f49a69f16d4f44439c9
Source noteuspto-grants-2014_03