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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452808Generated: October 29, 2026

Methylamine tetrahydrofuran → N-methyl-5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/452808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamine tetrahydrofuranHCID 66615946—
Reactant2-(Methylsulfonyl)-5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazoleHCID 68664235—
ProductN-methyl-5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazol-2-amineHCID 6866339467%

Reaction Steps

In the same manner as in Example 110 and using 2-(methylsulfonyl)-5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole instead of 2-(2,3-dihydro-1-benzofuran-5-yl)-5-(methylsulfonyl)-1,3,4-oxadiazole and using 2M methylamine-tetrahydrofuran solution instead of 3-fluorobenzylalcohol, the title compound (yield 67%) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-24028166b4b04c53905fdc5c58071261
Source noteuspto-grants-2013_07