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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875874Generated: October 30, 2026

Pyridine → HCID 71257392, compound

https://huagongshe.com/reaction/875874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantLithium HydroxideHCID 3939—
ReactantIsobutyryl chlorideHCID 62325—
ReactantHCID 67081885HCID 67081885—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 71257392HCID 7125739251%

Reaction Steps

Pyridine (1 mL) and isobutyryl chloride (0.421 g, 3.95 mmol) were added to (R)-tert-butyl 1-(3-amino-5-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl(methyl)carbamate (0.300 g, 0.790 mmol; Example 112, Step A) in NMP (2 mL), and the reaction was stirred at room temperature for 1 hour. 3M aqueous LiOH (3 mL) was then added, and the reaction was stirred for 10 minutes. Water (10 mL) and DCM (10 mL) were then added, and the organic layer was separated, dried, filtered and concentrated. The crude residue was purified by reverse phase chromatography (Biotage SP4, C-18 12M+, 5-95% CH3CN/water) to give (R)-tert-butyl 1-(5-chloro-3-isobutyramido-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl(methyl)carbamate (0.180 g, 51% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981085B2
Source datasetuspto-grants-2015_03
ORD IDord-275d2b13a39045edaca723db8c8488d2
Source noteuspto-grants-2015_03