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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807697Generated: October 29, 2026

Ammonia → HCID 58092735, compound

https://huagongshe.com/reaction/1807697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Bromo-5-(methoxymethoxy)pyridineHCID 57433666—
ReactantHCID 178418310HCID 178418310—
ReactantHCID 178418546HCID 178418546—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58092735HCID 58092735—

Reaction Steps

6.69 g (74.7 mmol) copper(I)cyanide in 15 ml dry THF was cooled to −75° C., where 149 ml (149 mmol) of a 1M tert-butylmagnesium chloride solution was added drop-wise. Stirring was continued for 40 min. After that, 4.07 g (18.67 mmol) 2-bromo-5-methoxymethoxy-pyridine (Zhong, W. et al. WO2008147547) dissolved in 30 ml dry THF were added drop-wise. The reaction mixture was stirred at −75° C. for 1 h and then allowed to reach room temperature, where stirring was continued for another 6 h. Then 30 ml of 25% aqueous ammonia was added to the reaction mixture. The mixture was filtered and extracted twice with CH2Cl2. The combined organic layers were washed with water, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by chromatography on silicagel (EtOAc, heptane) to yield 2.64 g of the pure title compound as an oil. LCMS: tR=0.55 min, M+H=196 (method K).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357707B2
Source datasetuspto-grants-2013_01
ORD IDord-650908670b2c4181a7fcb27627776ddc
Source noteuspto-grants-2013_01