Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522185Generated: November 3, 2026

Acryloyl chloride → HCID 86721786, compound

https://huagongshe.com/reaction/1522185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ReactantB-[4-[3-(Trifluoromethyl)phenoxy]phenyl]boronic acidHCID 57978431—
ProductHCID 86721786HCID 86721786—

Reaction Steps

1-(4-(((6-amino-5-(4-(3-(trifluoromethyl)phenoxy)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-(3-(trifluoromethyl)phenoxy)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 8.36 (s, 1H), 7.68 (t, 1H), 7.55 (d, 1H), 7.50-7.39 (m, 2H), 7.29 (dd, 4H), 7.08 (bs, 1H), 6.93 (bs, 2H), 6.78 (dd, 1H), 6.07 (dd, 1H), 5.64 (dd, 1H), 4.37 (d, 1H), 4.01 (d, 1H), 3.24 (t, 2H), 3.06-2.91 (m, 1H), 2.60 (t, 1H), 1.83 (bs, 1H), 1.62 (d, 2H), 0.98 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-431f955c8a0b4475abb01762ea99b08d
Source noteuspto-grants-2015_07