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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902006Generated: October 29, 2026

N-bromobutanimide → HCID 59700618, compound

https://huagongshe.com/reaction/902006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(6-Methyl-pyridin-2-yl)-pyrazolo[1,5-a]pyridine-3-carboxylic acidHCID 59700606—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59700618HCID 5970061887.7%

Reaction Steps

A solution of 2-(6-methyl-pyridin-2-yl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid (0.92 g, 3.6 mmol), sodium bicarbonate (1.04 g, 12.4 mmol), and N-bromosuccinimide (0.71 g, 4.0 mmol) in DMF (25 mL) is stirred for 2 hours at room temperature. The reaction is then diluted with water (50 mL) and extracted with EtOAc (3×15 mL). The organic layer is washed with brine and dried over sodium sulfate. The solvent is removed in vacuo to afford 0.91 g (87%) of desired product as a dark green solid. UV (95% EtOH) λmax 282 nm (ε 12089), 233 nm (ε 21813). TOF MS ES+ exact mass calculated for C13H10BrN3 (p+1): m/z=288.0136. Found: 287.0058. Anal. Calcd for C13H10BrN3: C, 54.19; H, 3.50; N, 14.58. Found: C, 54.10; H, 3.60; N, 14.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365066B2
Source datasetuspto-grants-2008_04
ORD IDord-6976a574a4cb46b3a8cc11c7e580b99e
Source noteuspto-grants-2008_04