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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522170Generated: November 3, 2026

Acryloyl chloride → HCID 86721774, compound

https://huagongshe.com/reaction/1522170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ProductHCID 86721774HCID 86721774—

Reaction Steps

1-(4-(((6-amino-5-(4-(trifluoromethoxy)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-(trifluoromethoxy)phenyl)boronic acid, and acryloyl chloride in four steps according to general scheme 2, using methods I, C, D, and G. MS: m/z=422 [M+H]+. 1H-NMR (400 MHz, DMSO-d6) δ 8.36 (s, 1H), 7.53 (d, 2H), 7.41 (d, 2H), 7.12 (t, 1H), 6.99 (s, 2H), 6.78 (dd, 1H), 6.07 (dd, 1H), 5.65 (dd, 1H), 4.37 (d, 1H), 4.02 (d, 2H), 3.22 (t, 2H), 2.98 (t, 1H), 2.58 (t, 1H), 1.82 (s, 1H), 1.62 (d, 2H), 0.97 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-bbdb22aba8724173a6683b89b7308700
Source noteuspto-grants-2015_07