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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522165Generated: November 4, 2026

(R)-(+)-1-Boc-3-aminopyrrolidine → (R,E)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)pyrrolidin-1-yl)-4-(dimethylamino)but-2-en-1-one

https://huagongshe.com/reaction/1522165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant(2E)-4-(Dimethylamino)-2-butenoic acidHCID 14805664—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
Product(R,E)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)pyrrolidin-1-yl)-4-(dimethylamino)but-2-en-1-oneHCID 71092905—

Reaction Steps

(R,E)-1-(3-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)pyrrolidin-1-yl)-4-(dimethylamino)but-2-en-1-one was prepared from 5,6-dichloropyrimidin-4-amine, (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate, (4-phenoxyphenyl)boronic acid, and (E)-4-(dimethylamino)but-2-enoic acid using methods B, C, D and E. HPLC purity: 99%. MS: m/z=459 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-ff80ed9863d84d2b8514b7a4bebfe968
Source noteuspto-grants-2015_07