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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560005Generated: October 25, 2026

2-Aminothiazole → 4-Nitro-3-(tetrahydro-furan-2-ylmethoxy)-toluene

https://huagongshe.com/reaction/560005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTetrahydrofurfuryl alcoholHCID 7360—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
Reactant4-Methyl-2-(oxolan-2-ylmethoxy)anilineHCID 24699884—
Product1-[4-Methyl-2-(tetrahydro-furan-2-ylmethoxy)-phenyl]-3-thiazol-2-yl-ureaHCID 5973299571%
Product4-Nitro-3-(tetrahydro-furan-2-ylmethoxy)-tolueneHCID 6699934775%

Reaction Steps

4-Nitro-3-(tetrahydro-furan-2-ylmethoxy)-toluene (0.88 g, 75%) was prepared from tetrahydro-furan-2-ylmethanol and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 4-methyl-2-(tetrahydro-furan-2-ylmethoxy)-aniline (0.50 g, 65%) following general procedure C. 1-[4-Methyl-2-(tetrahydro-furan-2-ylmethoxy)-phenyl]-3-thiazol-2-yl-urea (236 mg, 71%) was prepared from 4-methyl-2-(tetrahydro-furan-2-ylmethoxy)-aniline (207 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 numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-5d1eba44fdd2427a9960d6c78cad70eb
Source noteuspto-grants-2011_11