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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520201Generated: November 2, 2026

N-bromobutanimide → HCID 86658556, compound

https://huagongshe.com/reaction/1520201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-(4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)thiazol-2-yl)pyridin-2-amineHCID 86642330—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
ProductHCID 86658556HCID 8665855696%

Reaction Steps

According to Scheme 5 Step 1: A solution of N-(4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)thiazol-2-yl)pyridin-2-amine (4.20 mmol, 1.53 g) and N-bromosuccinimide (4.40 mmol, 782 mg) in DMF (76 mL) was stirred for 1.5 hour at 50° C. The reaction mixture was diluted with a saturated solution of Na2CO3 and water. The precipitate formed was recovered and washed with DCM. The aqueous phase was extracted with DCM and the organic phase was washed. The organic phase was dried over MgSO4, was filtered and was concentrated to yield with the addition of the precipitate N-(4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-5-bromothiazol-2-yl)pyridin-2-amine (4.02 mmol, 1.78 g, 96%) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073907B2
Source datasetuspto-grants-2015_07
ORD IDord-aab2c10129b44404856c0bcb318415f5
Source noteuspto-grants-2015_07