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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388524Generated: October 26, 2026

Alloxan → 5-Hydroxy-5-(2-benzthiazolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione

https://huagongshe.com/reaction/1388524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAlloxanHCID 5781—
ReactantBenzothiazoleHCID 7222—
Product5-Hydroxy-5-(2-benzthiazolyl)-2,4,6-(1H,3H,5H)pyrimidinetrioneHCID 21271261—

Reaction Steps

By the procedure of Example 38, benzthiazole (2.7 g., 0.02 moles) was converted to its 2-lithio derivative and then reacted with anhydrous alloxan to yield title product, initially isolated as an oil. The latter was crystallized from ether-hexane [2.2 g.; Rf 0.55 (1:1 ethyl acetate:hexane/5% acetic acid)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431810
Source datasetuspto-grants-1984_02
ORD IDord-fb19ba302f2e48699792bf8bab5a893b
Source noteuspto-grants-1984_02