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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117516Generated: October 29, 2026

4-(1H-imidazol-1-yl)benzaldehyde → HCID 54139938, compound

https://huagongshe.com/reaction/2117516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1H-imidazol-1-yl)benzaldehydeHCID 736530—
ReactantMethyl 7-aminoheptanoate hydrochlorideHCID 13807349—
SolventMethanolHCID 887—
ProductHCID 54139938HCID 54139938—

Reaction Steps

The title compound of Step A was prepared from 7-amino-heptanoic acid methyl ester hydrochloride, of Preparation 1, and 4-imidazol-1-yl-benzaldehyde, of Preparation 43, using the method described in Example 1, Step A except that the mine was formed in MeOH with a reaction time of 1h. 1H NMR (400 MHz, CDCl3) δ 7.82 (m, 1H), 7.43 (d, 2H), 7.33 (d, 2H), 7.25 (m, 1H), 7.18 (m, 1H), 3.82 (s, 2H), 3.65 (s, 3H), 2.62 (t, 2H), 2.29 (t, 2H), 1.61 (m, 2H), 1.52 (m, 2H), 1.33 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442702B2
Source datasetuspto-grants-2008_10
ORD IDord-9eba4c931a0743cc98915695630a0762
Source noteuspto-grants-2008_10