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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522119Generated: November 4, 2026

2-Butynoic acid → HCID 71093010, compound

https://huagongshe.com/reaction/1522119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butynoic acidHCID 68535—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
CatalystLindlars catalystHCID 131709914—
ProductHCID 71093010HCID 71093010—

Reaction Steps

(Z)-1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)methyl)piperidin-1-yl)but-2-en-1-one was prepared from 5,6-dichloropyrimidin-4-amine, tert-butyl 4-(aminomethyl)piperidine-1-carboxylate, (4-phenoxyphenyl)boronic acid, and but-2-ynoic acid using methods B, C, D, E, and hydrogenation using Lindlar's catalyst. HPLC purity: 81%. MS: m/z=444 [M+H]+. 1H-NMR (DMSO-d6) □δ 8.35 (s, 1H), 7.45 (t, 2H), 7.28-6.95 (m, 10H), 6.06 (d, 1H), 5.94-5.86 (m, 1H), 4.35 (d, 1H), 3.83 (d, 1H), 3.24 (m, 2H), 2.94 (t, 1H), 2.55 (t, 1H), 1.82-1.74 (m, 4H), 1.61 (d, 2H), 0.96 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-ddf660daafba4416af5bc4b4da9768b9
Source noteuspto-grants-2015_07