Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485499Generated: October 31, 2026

6-(4-Ethylpiperazin-1-yl)pyridin-3-amine → N-(3-(4-amino-2-(6-(4-ethylpiperazin-1-yl)pyridin-3-ylamino)thieno[3,2-d]pyrimidin-7-yl)phenyl)methanesulfonamide

https://huagongshe.com/reaction/1485499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Ethylpiperazin-1-yl)pyridin-3-amineHCID 9161674—
ReactantN-(3-(4-amino-2-chlorothieno[3,2-d]pyrimidin-7-yl)phenyl)methanesulfonamideHCID 86675656—
ProductN-(3-(4-amino-2-(6-(4-ethylpiperazin-1-yl)pyridin-3-ylamino)thieno[3,2-d]pyrimidin-7-yl)phenyl)methanesulfonamideHCID 5323865774.9%

Reaction Steps

The target compound of Example 27 (22 mg, 74% yield) was prepared in the same manner as Step 9 of Example 1 using N-(3-(4-amino-2-chlorothieno[3,2-d]pyrimidin-7-yl)phenyl)methanesulfonamide (20 mg, 0.056 mmol) and 6-(4-ethylpiperazin-1-yl)pyridin-3-amine (31 mg, 0.17 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422307B2
Source datasetuspto-grants-2016_08
ORD IDord-95e9135a48264c79843d8c0d9b1a0d07
Source noteuspto-grants-2016_08