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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65677Generated: October 26, 2026

4,5-Dihydro-2-thiazolamine → 2,3,8,9-Tetrahydro-5-(4-methoxy-2,5-dimethylphenyl)-9-[(4-methoxy-2,5-dimethylphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidine

https://huagongshe.com/reaction/65677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5-Dihydro-2-thiazolamineHCID 15689—
ReactantTetrahydro-3,5-bis[(4-methoxy-2,5-dimethylphenyl)methylene]-4H-pyran-4-oneHCID 53782418—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product2,3,8,9-Tetrahydro-5-(4-methoxy-2,5-dimethylphenyl)-9-[(4-methoxy-2,5-dimethylphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidineHCID 2178668246.9%

Reaction Steps

A stirred solution of tetrahydro-3,5-bis[(4-methoxy-2,5-dimethylphenyl)methylene]-4H-pyran-4-one (3.0 g, 7.6 mmole) and 2-amino-2-thiazoline (1.0 g, 9.7 mmole) in 75 ml of CHCl3 is heated at reflux temperature for 72 hours. After cooling, the solution is filtered to remove a small amount of insoluble material. The solvent is evaporated to give an oily residue. A solution of this material in 25 ml of EtOH yields 1.7 g of light yellow solid, m.p. 195°-197°. Crystallization from 20 ml of 10% DMF/MeOH gives 1.3 g (35%) of cream colored solid, m.p. 196°-198°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128648
Source datasetuspto-grants-1978_12
ORD IDord-f8d52a0270014774bde0a6d1b66b7a76
Source noteuspto-grants-1978_12