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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564781Generated: October 31, 2026

4-Chlorothieno[3,2-d]pyrimidine → HCID 22112850, compound

https://huagongshe.com/reaction/564781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
ReactantHCID 19626987HCID 19626987—
SolventIsopropanolHCID 3776—
ProductHCID 22112850HCID 2211285078%

Reaction Steps

4-Chlorothieno[3,2-d]pyrimidine (0.102 g, 0.60 mmol) and 3-chloro-4-(2-methoxybenzyloxy)aniline (prepared according to the published method: WO 96/09294) (0.161 g, 0.65 mmol) were reacted in 2-propanol (4 ml) for 1.25 hours, according to Procedure A. The product was obtained as pale cream prisms (0.203 g, 78%) with m.p. 210-212° C.; (Found: C, 55.28; H, 4.00; N, 9.44. C20H16ClN3O2S.HCl requires: C, 55.31; H, 3.92; N, 9.67%); δH [2H6]-DMSO 11.19 (1H, br s, NH), 8.88 (1H, s, 2-H), 8.48 (1H, d, J 7, 6 H or 7 H) 7.87 (1H, d, J 5, 2′-H), 7.55-7.62 (2H, m, 6′-H, 4″-H), 7.48 (1H, d, J 7, 6H or 7H), 7.28-7.40 (2H, m, 5′-H, 6″-H), 7.09 (1H, d, J 9, 3″-H), 7.00 (1H, t, J 9, 5″-H), 5.22 (2H, s, CH2), 3.85 (3H, s, OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169091A
Source datasetuspto-grants-2001_01
ORD IDord-12ffbe29f41741e9b49370dbe20c51dc
Source noteuspto-grants-2001_01