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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190213Generated: October 28, 2026

2-Amino-6-methylpyridine → HCID 178425538, compound

https://huagongshe.com/reaction/1190213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-methylpyridineHCID 15765—
ReactantHCID 178424524HCID 178424524—
ProductHCID 178425538HCID 178425538—

Reaction Steps

The title compound was prepared from 4-cyano-1H-imidazole-2-carboxylic acid [2-(4,4-dimethyl-cyclohex-1-enyl)-4-(1-hydroxy-1-methyl-ethyl)-phenyl]-amide (as prepared in Example 14, step (d)) and 2-amino-6-methylpyridine using the conditions described in Example 72. 1H-NMR (CDCl3-CD3OD; 400 MHz): δ 8.26 (dd, 1H, J=8.6, 2.0 Hz), 7.76 (s, 1H), 7.54-7.49 (m, 1H), 7.28-7.22 (m, 1H), 7.14 (d, 1H, J=2.2 Hz), 6.58 (d, 1H, J=7.3 Hz), 6.07 (m, 1H), 5.67 (m, 1H), 2.46 (s, 3H), 2.20-2.14 (m, 2H), 2.00 (m, 2H), 1.71 (s, 6H), 1.51-1.48 (m, 2H), 1.00 (s, 6H). Mass spectrum (ESI, m/z): Calcd. for C28H32N6O, 469.2 (M+H). found 469.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674100B2
Source datasetuspto-grants-2014_03
ORD IDord-5789429ff34f42da880e64752d765b33
Source noteuspto-grants-2014_03