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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536981Generated: October 30, 2026

HCID 68860672, compound → HCID 178424472, compound

https://huagongshe.com/reaction/536981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68860672HCID 68860672—
Reactant4-Cyano-1H-imidazole-2-carboxylic acid [4-bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenyl]-amideHCID 178424443—
ProductHCID 178424472HCID 178424472—

Reaction Steps

The title compound was prepared as described in Example 1, step (h) using 4-cyano-1H-imidazole-2-carboxylic acid [4-bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenyl]-amide (as prepared in Example 1, step (g)) and 1,5-dimethyl-8-oxa-bicyclo[3.2.1]octan-3-one (J. Org. Chem., 64(10), 3398-3408 (1999)). 1H-NMR (DMSO-d6; 400 MHz): d 14.25 (bs, 1H), 9.72 (s, 1H), 8.29 (s, 1H), 7.90 (d, 1H, J=8.3 Hz), 7.33 (dd, 1H, J=2.3, 8.6 Hz), 7.27 (m, 1H), 5.65 (m, 1H), 4.88 (s, 1H), 2.42-2.37 (m, 2H), 2.26-2.22 (m, 2H), 1.95 (m, 2H), 1.81-1.71 (m, 4H), 1.53-1.47 (m, 4H), 1.23 (s, 6H), 1.00 (s, 6H). Mass spectrum (ESI, m/z): Calcd. for C28H34N4O3, 475.2 (M+1). found 475.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859602B2
Source datasetuspto-grants-2014_10
ORD IDord-6d32c07932a240d48ec66073c33cb101
Source noteuspto-grants-2014_10