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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042223Generated: November 1, 2026

2-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol → N-Cyclopropyl-3-(2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thieno[3,2-d]pyrimidin-7-yl)benzamide

https://huagongshe.com/reaction/2042223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanolHCID 14479558—
Reactant3-(2-aminothieno[3,2-d]pyrimidin-7-yl)-N-cyclopropylbenzamideHCID 67120144—
ProductN-Cyclopropyl-3-(2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thieno[3,2-d]pyrimidin-7-yl)benzamideHCID 5293189547.1%

Reaction Steps

N-Cyclopropyl-3-(2-(6-(4-(2-hydroxyethyl)piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thieno[3,2-d]pyrimidin-7-yl)benzamide (16 mg, 47% yield) was prepared in the same manner as Step 10 of Example 1 using 3-(2-aminothieno[3,2-d]pyrimidin-7-yl)-N-cyclopropylbenzamide (20 mg, 0.064 mmol) and 2-(4-(6-chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol (17 mg, 0.064 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586580B2
Source datasetuspto-grants-2013_11
ORD IDord-14a5f28c3fa14b77a9a3dc11bcc7b89a
Source noteuspto-grants-2013_11