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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564783Generated: October 31, 2026

4-Chlorothieno[3,2-d]pyrimidine → HCID 22112857, compound

https://huagongshe.com/reaction/564783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
ReactantHCID 22112878HCID 22112878—
SolventIsopropanolHCID 3776—
ProductHCID 22112857HCID 2211285782%

Reaction Steps

4-Chlorothieno[3,2-d]pyrimidine (0.102 g, 0.60 mmol) and 3-methoxy-4-(2-methoxybenzyloxy)aniline (prepared according to the published method: WO 96/09294) (0.181 g, 0.70 mmol) were reacted in 2-propanol (3 ml) for 75 minutes according to Procedure A. The product was obtained as off-white prisms (0.211 g, 82%) with m.p. 207-208° C.; (Found: C, 58.55; H, 4.76; N, 9.53. C21H19N3O3S.HCl requires: C, 58.55; H, 4.69; N, 9.77%); δH [2H6]-DMSO 8.85 (1H, s, 2-H), 8.41 (1H, d, J 7, 6 H or 7 H) 7.55 (1H, d, J 7, 6-H or 7-H), 7.42 (1H, d, J 9, 6′-H), 7.34 (1H, t, J 8, 4″-H), 7.29 (1H, s, 2′-H), 7.02-7.20 (3H, m, 5′-H, 3″-H, 6″-H), 6.98 (1H, t, J 8, 5″-H), 5.08 (2H, s, CH2), 3.83 and 3.79 (2x 3H, 2 x s, 2 x OCH3); m/z 393 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169091A
Source datasetuspto-grants-2001_01
ORD IDord-14b2c87ed2e7419aa4bdb9bc5c8d5634
Source noteuspto-grants-2001_01