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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102822Generated: October 30, 2026

N-(6-amino-1,3-benzothiazol-2-yl)benzamide → N-[6-(Purin-6-ylamino)benzothiazol-2-yl]benzamide

https://huagongshe.com/reaction/2102822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(6-amino-1,3-benzothiazol-2-yl)benzamideHCID 810331—
Reactant6-ChloropurineHCID 5359277—
SolventEthanolHCID 702—
ProductN-[6-(Purin-6-ylamino)benzothiazol-2-yl]benzamideHCID 23132486—

Reaction Steps

N-[6-(Purin-6-ylamino)benzothiazol-2-yl]benzamide was prepared by heating a mixture of N-(6-aminobenzothiazol-2-yl)benzamide (IM 2, 50 mg, 0.186 mmol) and 6-chloropurine (29 mg, 0.186 mmol) in ethanol (3 ml) to 80° C. for 4 h. The resulting precipitate was separated by filtration and washed with ethanol (69 mg, 0.178 mmol, 96%). LC/ESI-MS: m/z 388 [M+H]+; m/z=386 [M−H]−; Rt=3.07 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576090B2
Source datasetuspto-grants-2009_08
ORD IDord-12504510e94a4259b7c77e7e1b9fe7be
Source noteuspto-grants-2009_08