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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102823Generated: October 30, 2026

Dimethylformamide → N-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-ylamino]benzothiazol-2-yl}benzamide

https://huagongshe.com/reaction/2102823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDichloromethaneHCID 6344—
ReactantN-(6-amino-1,3-benzothiazol-2-yl)benzamideHCID 810331—
Reactant2-Chloro-4-(4-methylpiperazin-1-yl)pyrimidineHCID 1714225—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductN-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-ylamino]benzothiazol-2-yl}benzamideHCID 23132480—

Reaction Steps

N-{6-[4-(4-Methylpiperazin-1-yl)pyrimidin-2-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 2-chloro-4-(4methylpiperazin1-yl)pyrimidine (IM 10, 40 mg, 0.186 mmol) in ethanol (3 mL) to 80° C. for 4 days. After dissolving the precipitate by addition of dimethylformamide, pTLC (dichloromethane:methanol=4.1) yielded a solid (44 mg, 0.100 mmol, 54%). LC/ESI-MS: m/z=446 [M+H]+; m/z=444 [M−H]−; Rt=2.12 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576090B2
Source datasetuspto-grants-2009_08
ORD IDord-59a2a14b3c344cafb1c03889e0e253c4
Source noteuspto-grants-2009_08