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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500848Generated: October 25, 2026

4-Chlorothieno[3,2-d]pyrimidine → 4-Chlorothieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/500848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
Reactantthieno(2,3-d)pyrimidin-4(3H)-oneHCID 2808547—
Product4-Chlorothieno[2,3-d]pyrimidineHCID 73661893%

Reaction Steps

Starting from thieno[2,3-d]pyrimidin-4(3H)-one (204) [J. Med. Chem., 1999, 42, 26, 5437-5447, Bull. Soc. Chim. Fr., 1975, 587-591] and following the procedure described above for the synthesis of compound 20 (scheme 4, example 22), title compound 205 was obtained in 93% yield. LRMS (M+1) 169.1 (100%), 171.1 (32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-ce5cd134ddeb415897b312bb36ccb222
Source noteuspto-grants-2010_08