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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276256Generated: October 25, 2026

2-Aminothiazole → 4-(2-Methylpropoxy)-3-nitrobenzaldehyde

https://huagongshe.com/reaction/2276256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantIsobutanolHCID 6560—
Reactant4-Fluoro-3-nitrobenzaldehydeHCID 598129—
Reactant5-Formyl-2-(2-methylpropoxy)anilineHCID 82057088—
Product4-(2-Methylpropoxy)-3-nitrobenzaldehydeHCID 2882948175%
Product1-(5-Formyl-2-isobutoxy-phenyl)-3-thiazol-2-yl-ureaHCID 5973278565%

Reaction Steps

4-(2-Methylpropoxy)-3-nitrobenzaldehyde (0.83 g, 75%) was prepared from 2-methyl-propanol (0.46 ml, 5.0 mmol) and 4-fluoro-3-nitrobenzaldehyde (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 5-formyl-2-(2-methylpropoxy)-aniline (0.49 g, 68%) following general procedure B. 1-(5-Formyl-2-isobutoxy-phenyl)-3-thiazol-2-yl-urea (208 mg, 65%) was prepared from 5-formyl-2-(2-methylpropoxy)aniline (193 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-2115c5c94a374d91a6e762878d7a2bf6
Source noteuspto-grants-2015_09