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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34462Generated: October 25, 2026

Guanidine Hydrochloride → 2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine

https://huagongshe.com/reaction/34462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantBenzenamine hydrochloride (1:1)HCID 8870—
ReactantSodium MethoxideHCID 10942334—
Reactant2-(7,8-Dimethoxy-2H-1-benzopyran-5-ylmethyl)-3-morpholino acrylonitrileHCID 54280763—
Product2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidineHCID 1284977242.7%

Reaction Steps

2-(7,8-Dimethoxy-2H-1-benzopyran-5-ylmethyl)-3-morpholino acrylonitrile (562 g, 1.64 mol) and aniline hydrochloride (234 g, 1.80 mol) were refluxed in SD3A (2.4 L) for one hour. The reaction was cooled, and guanidine hydrochloride (313 g, 3.28 mol) and sodium methoxide (275 g, 5.08 mol) were added. After continued reflux, the product crystallized from the cooled reaction mixture. Filtration followed by water wash (2 L) gave 2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine (220 g, 42.7%). Crystallization from ethanol-water gave title compound, mp 235°-238°, identical to the product of Example 1C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761475
Source datasetuspto-grants-1988_08
ORD IDord-cee52d64b5dc4625a65ee23e86a5187e
Source noteuspto-grants-1988_08