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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564789Generated: November 1, 2026

4-Chlorothieno[3,2-d]pyrimidine → HCID 22112870, compound

https://huagongshe.com/reaction/564789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
Reactant4-(Cyclohexylmethoxy)anilineHCID 15681651—
SolventIsopropanolHCID 3776—
ProductHCID 22112870HCID 2211287068%

Reaction Steps

4-Chlorothieno[3,2-d]pyrimidine (0.171 g, 1.00 mmol) and 4-cyclohexylmethoxy-aniline (prepared according to the published method: WO 96/09294) (0.205 g, 1.00 mmol) were reacted in 2-propanol (5 ml) for 5 hours, according to Procedure A. The product was obtained as cream prisms (0.255 g, 68%) with m.p. 232-233° C.; (Found: C, 60.65; H, 5.68; N, 11.25. C19H21N3OS.HCl requires: C, 60.71; H, 5.90; N, 11.23%); δH [2H6]-DMSO 11.11 (1H, br s, NH), 8.71 (1H, s, 2-H), 8.41 (1H, d, J 7,6 H or 7 H) 7.44-7.58 (3H, m, 6H or 7H, 2′-H, 6′-H), 7.03 (2H, d, J 9, 3′-H, 5′-H), 3.84 (2H, s, CH2), 1.58-1.90 (6H, m) and 0.98-1.33 (5H, m) (cyclohexyl-H11); m/z 339 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169091A
Source datasetuspto-grants-2001_01
ORD IDord-1292bf54059e4a298f5a7b74815bba34
Source noteuspto-grants-2001_01