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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520209Generated: November 4, 2026

Chlorosuccinimide → HCID 86658562, compound

https://huagongshe.com/reaction/1520209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 86658563HCID 86658563—
SolventDimethylformamideHCID 6228—
ProductHCID 86658562HCID 8665856251.6%

Reaction Steps

According to Scheme 7, Step 1: To a solution of 4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-N-(pyrimidin-2-yl)thiazol-2-amine (0.85 mmol, 0.31 g) in DMF (1 mL) was added 1-chloropyrrolidine-2,5-dione (0.64 mmol, 85 mg). The reaction mixture was stirred for 1 hour at room temperature. The reaction was quenched with a saturated aqueous solution of Na2CO3 and extracted with AcOEt. The combined organic layers were dried over MgSO4, were filtered and were evaporated under reduced pressure to afford 5-chloro-4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-N-(pyrimidin-2-yl)thiazol-2-amine (0.33 mmol, 130 mg, 38%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073907B2
Source datasetuspto-grants-2015_07
ORD IDord-b28c6d990e464208a1689a32ed1b43fa
Source noteuspto-grants-2015_07