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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660141Generated: October 25, 2026

3-Pyridineacetic acid → HCID 12999592, compound

https://huagongshe.com/reaction/660141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridineacetic acidHCID 108—
ReactantMethoxy-methyl amideHCID 53630747—
ReactantButyllithiumHCID 178418339—
ProductHCID 12999592HCID 12999592—

Reaction Steps

In another example of the general procedure (scheme 2), readily available pyridin-3-yl-acetic acid (10) is converted to the N-methyl-N-methoxyamide derivate (12), which is reacted with BuLi to produce 1-pyridin-3-yl-hexan-2-one (13). N,N-dimethylformamide dimethylacetal treatment of 13 furnished the enamine (14) which is converted to the pyrazol (15). The synthesis of 3-(4-Butyl-1H-pyrazol-3-yl)-1,2,5,6-tetrahydro-1-methylpyridine (16) is illustrated in scheme 2 according to the two step sequence shown in scheme 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084473B2
Source datasetuspto-grants-2011_12
ORD IDord-c7300da0306f4503aa3ababc126f085b
Source noteuspto-grants-2011_12