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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276249Generated: October 29, 2026

2-Aminothiazole → 2-(Cyclopropylmethoxy)-4-methyl-1-nitrobenzene

https://huagongshe.com/reaction/2276249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
ReactantCyclopropanemethanolHCID 75644—
Reactant2-(Cyclopropylmethoxy)-4-methylanilineHCID 43560040—
ProductHCID 59732787HCID 5973278772%
Product2-(Cyclopropylmethoxy)-4-methyl-1-nitrobenzeneHCID 6699887375%

Reaction Steps

3-Cyclopropylmethoxy-4-nitrotoluene (0.77 g, 75%) was prepared from cyclopropylmethanol and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 2-cyclopropylmethoxy-4-methyl-aniline (0.47 g, 71%) following general procedure C. 1-(2-Cyclopropylmethoxy-4-methyl-phenyl)-3-thiazol-2-yl-urea (218 mg, 72%) was prepared from 2-cyclopropylmethoxy-4-methyl-aniline (177 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-9e2ce1c996b4415b94c96c27c10ef27c
Source noteuspto-grants-2015_09