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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628105Generated: November 3, 2026

Cyclohexanecarbonyl chloride → HCID 58009940, compound

https://huagongshe.com/reaction/1628105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
Reactant(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methanamine hydrochlorideHCID 67068339—
SolventDichloromethaneHCID 6344—
ProductHCID 58009940HCID 5800994039.4%

Reaction Steps

To a suspension of crude (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methanamine hydrochloride (assumed 0.498 mmol) in DCM (10 mL) was added TEA (0.208 mL, 1.49 mmol) followed by cyclohexanecarbonyl chloride (0.101 mL, 0.747 mmol). The mixture was stirred for 30 min at rt and then was diluted with DCM and washed with saturated aqueous NaHCO3 (25 mL) and brine (25 mL). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The material was purified by silica gel chromatography eluting with a gradient of 40 to 80% EtOAc in DCM to provide N-((5-Tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)methyl)cyclohexanecarboxamide as a tan solid (0.081 g, 39%). LC/MS (Table 2, Method a) Rt=2.40 min; MS m/z: 413 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785639B2
Source datasetuspto-grants-2014_07
ORD IDord-24495ad729bd4b60b4634b8d5ce58c78
Source noteuspto-grants-2014_07