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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522180Generated: November 5, 2026

Acryloyl chloride → HCID 86721782, compound

https://huagongshe.com/reaction/1522180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
Reactant(4-Phenoxy-2-(trifluoromethyl)phenyl)boronic acidHCID 71092794—
ProductHCID 86721782HCID 86721782—

Reaction Steps

1-(4-(((6-amino-5-(4-phenoxy-2-(trifluoromethyl)phenyl)pyrimidin-4-yl)amino)methyl)piperidin-1-yl)prop-2-en-1-one was prepared from 5,6-dichloropyrimidin-4-amine, tert-butyl 4-(aminomethyl)piperidine-1-carboxylate, (4-phenoxy-2-(trifluoromethyl)phenyl)boronic acid, and acryloyl chloride in four steps according to general scheme 2, using methods I, C, D and G. MS: m/z=498 [M+H]+. 1H-NMR (400 MHz, DMSO-d6) δ 8.35 (s, 1H), 7.50 (dd, 2H), 7.39 (m, 2H), 7.28 (t, 1H), 7.19 (d, J=7.8 Hz, 2H), 7.16-7.07 (m, 1H), 7.00 (bs, 1H), 6.78 (dd, 1H), 6.06 (dd, 1H), 5.64 (dd, 1H), 4.36 (d, 1H), 4.01 (d, 1H), 3.16 (m, 2H), 2.97 (t, 1H), 2.65-2.54 (t, 1H), 1.78 (bs, 1H), 1.58 (bs, 2H), 0.97 (bs, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-95f54cf4ddcb4e8c95748633cff58c1f
Source noteuspto-grants-2015_07