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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723112Generated: November 1, 2026

3-Pyridinemethanamine → HCID 14518368, compound

https://huagongshe.com/reaction/1723112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanamineHCID 31018—
ReactantHCID 14990940HCID 14990940—
SolventEthanolHCID 702—
ProductHCID 14518368HCID 1451836882%

Reaction Steps

(a-3) A mixture of 4.4 parts of 1-[(4-fluoro-3-nitrophenyl)methyl]-1H-imidazole, 4.33 parts of 3-pyridinemethanamine and 80 parts of absolute ethanol was stirred for 4 hours at reflux temperature. The reaction mixture was evaporated. 50 Parts of water were added to the residue. The product was extracted twice with 130 parts of trichloromethane. The combined trichloromethane layers were dried, filtered and evaporated. The residue was crystallized from 48 parts of 2-propanol. The product was filtered off and dried, yielding 5.1 parts (82%) of N-[4-(1H-imidazol-1-ylmethyl)-2-nitrophenyl]-3-pyridinemethanamine; mp. 171.0° C. (int. 71).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859684
Source datasetuspto-grants-1989_08
ORD IDord-c9cc5607ce1147c9b3579884467ba095
Source noteuspto-grants-1989_08