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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500826Generated: October 25, 2026

2-Fluoro-4-nitrophenol → 4-(3-Chloro-4-nitrophenoxy)thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/500826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-nitrophenolHCID 9825—
Reactant3-Chloro-4-nitrophenolHCID 10283—
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
Reactant4-(2-Fluoro-4-nitrophenoxy)-N-(2-morpholinoethyl)thieno[3,2-d]pyrimidine-6-carboxamideHCID 59424553—
Product4-(3-Chloro-4-nitrophenoxy)thieno[3,2-d]pyrimidineHCID 4744636272%

Reaction Steps

Starting from the chloride 20 (scheme 4) and following the procedure described above for the synthesis of compound 24 (scheme 4, example 22) remplacing 2-fluoro-4-nitrophenol with 3-chloro-4-nitrophenol, title compound 171 was obtained in 72% yield. LRMS (M+1) 307.7 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-5512f104ab1a4b8dbb0cca2b407814ff
Source noteuspto-grants-2010_08