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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522287Generated: November 4, 2026

1-Piperidinepropanoic acid → HCID 71093019, compound

https://huagongshe.com/reaction/1522287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Piperidinepropanoic acidHCID 117782—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactanttrans-1-Boc-4-aminomethyl-3-hydroxypiperidineHCID 11075229—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ProductHCID 71093019HCID 7109301924.2%

Reaction Steps

1-((3S,4S)-4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)methyl)-3-hydroxypiperidin-1-yl)-3-(piperidin-1-yl)propan-1-one was prepared 5,6-dichloropyrimidin-4-amine, 4-phenoxyphenylboronic acid, (3S,4S)-tert-butyl 4-(aminomethyl)-3-hydroxypiperidine-1-carboxylate and 3-(piperidin-1-yl)propanoic acid with method S1, S2, S3, S4A. Yield 24.2%. 1H NMR (CD3OD) δ 8.26 (s, 1H), 7.14-7.40 (m, 9H), 4.48 (dd, 1H), 3.89 (t, 1H), 3.67 (t, 1H), 3.28 (m, 1H), 3.00 (m, 1H), 2.31-2.61 (m, 8H), 1.75 (m, 5H), 1.49 (s, 2H), 1.20 (m, 1H). HPLC PURITY: 99%, MS: m/z=530[M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-80aeabf58de2498198fa8a279b9f2e0c
Source noteuspto-grants-2015_07