Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522128Generated: November 3, 2026

3-Aminophenol → HCID 178426212, compound

https://huagongshe.com/reaction/1522128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
Reactant(E)-4-(4-(tert-butoxycarbonyl)piperazin-1-yl)but-2-enoic acidHCID 71092896—
ReactantHCID 178426214HCID 178426214—
ProductHCID 178426212HCID 178426212—

Reaction Steps

(E)-7-(3-(4-(4-((3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)oxy)phenyl)amino)-4-oxobut-2-en-1-yl)piperazin-1-yl)-3-oxopropyl)-5,5-difluoro-1,3-dimethyl-5H-dipyrrolo[1,2-c:2′,1′-f][1,3,2]diazaborinin-4-ium-5-uide was prepared from 5,6-dichloropyrimidin-4-amine, 3-aminophenol, (4-phenoxyphenyl)boronic acid, (E)-4-(4-(tert-butoxycarbonyl)piperazin-1-yl)but-2-enoic acid, and 7-(2-carboxyethyl)-5,5-difluoro-1,3-dimethyl-5H-dipyrrolo[1,2-c:2′,1′-f][1,3,2]diazaborinin-4-ium-5-uide using methods A, B, E, D, and E. HPLC purity: 100%. MS: m/z=797 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-ea92195cb9454ed8a52df4993c27a8f2
Source noteuspto-grants-2015_07