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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391048Generated: October 30, 2026

(2-Aminopyrimidin-5-yl)boronic acid → HCID 58234065, compound

https://huagongshe.com/reaction/391048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Aminopyrimidin-5-yl)boronic acidHCID 17750211—
ReactantHCID 87209431HCID 87209431—
SolventDiethyl EtherHCID 3283—
ProductHCID 58234065HCID 58234065—

Reaction Steps

(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-(1-isopropyl-piperidin-4-yl)-(2-methoxy-ethyl)-amine was reacted with 2-aminopyrimidine-5-boronic acid in General Procedure A. Acid/base work-up and trituration with ether yielded 334. 400 MHz, 1H NMR CDCl3: 9.30 (s, 2H), 7.26 (s, 1H), 5.22 (br s, 2H, NH2), 4.06 (s, 2H), 4.05 (t, 4H, J 4.4), 3.90 (t, 4H, J4.6), 3.50 (t, 2H, J6.0), 3.32 (s, 3H), 2.94 (d, 2H, J 11.2), 2.85 (t, 2H, J 6.1), 2.75-2.68 (m, 1H), 2.61-2.55 (m, 1H), 2.10 (t, 2H, J 11.4), 1.85 (d, 2H, J12.0), 1.65-1.53 (m, 2H), 1.03 (d, 6H, J 6.4). LC-MS (m+1)=527.41

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-f1cdadc7fef141909d6955bbd964e2fc
Source noteuspto-grants-2013_02