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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522148Generated: November 2, 2026

Acryloyl chloride → HCID 86721761, compound

https://huagongshe.com/reaction/1522148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactanttert-Butyl 4-((methylamino)methyl)piperidine-1-carboxylateHCID 21934652—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ProductHCID 86721761HCID 86721761—

Reaction Steps

1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)(methyl)amino)methyl)piperidin-1-yl)prop-2-en-1-one was prepared from 5,6-dichloropyrimidin-4-amine, tert-butyl 4-((methylamino)methyl)piperidine-1-carboxylate, (4-phenoxyphenyl)boronic acid, and acryloyl chloride using methods B, C, D, and F. HPLC purity: 100%. MS: m/z=444 [M+H]+. 1H-NMR (DMSO-d6) δ 8.32 (s, 1H), 7.45 (t, 2H), 7.33 (d, 2H), 7.20 (t, 1H), 7.12 (t, 4H), 6.95 (broad s, 1.5H), 6.77 (dd, 1H), 6.07 (d, 1H), 5.65 (d, 1H), 4.38 (d, 1H), 4.01 (d, 1H), 3.36 (m, 2H), 2.99 (t, 1H), 2.68 (s, 3H), 2.57 (t, 1H), 1.92 (s, 1H), 1.50 (d, 2H), 0.97 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-8f1a61bbc60143589b40c2a80f648bc0
Source noteuspto-grants-2015_07