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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391013Generated: October 29, 2026

2-Aminopyrimidine-5-boronic acid, pinacol ester → 5-(4-Morpholino-6-(1-(4-n-methylsulfonylpiperazin-1-yl)ethyl)thieno[3,2-d]pyrimidin-2-yl)pyrimidin-2-amine

https://huagongshe.com/reaction/391013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminopyrimidine-5-boronic acid, pinacol esterHCID 17750212—
Reactant2-Chloro-6-[1-(4-methanesulfonyl-piperazin-1-yl)-ethyl]-4-morpholin-4-yl-thieno[3,2-d]pyrimidineHCID 86618431—
Product5-(4-Morpholino-6-(1-(4-n-methylsulfonylpiperazin-1-yl)ethyl)thieno[3,2-d]pyrimidin-2-yl)pyrimidin-2-amineHCID 58234066—

Reaction Steps

2-Chloro-6-[1-(4-methanesulfonyl-piperazin-1-yl)-ethyl]-4-morpholin-4-yl-thieno[3,2-d]pyrimidine was reacted with 2-aminopyrimidine-5-boronic acid pinacol ester in General Procedure A. Purification on silica yielded 300. NMR: (CDCl3): 1.44 (3 H, d, J 7.1, Me), 2.52-2.64 (4 H, m, CH2), 2.73 (3 H, s, Me), 3.21-3.23 (4 H, m, CH2), 3.80-3.83 (4 H, m, CH2), 3.94-4.06 (5 H, m), 5.16 (2 H, s, NH2) and 9.20 (2 H, s, Ar). MS: (ESI+): MH+=505.20

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-c14a682a3e6643de93e9126859e2f670
Source noteuspto-grants-2013_02