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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522277Generated: November 3, 2026

1-Boc-4-(aminomethyl)piperidine → HCID 71093037, compound

https://huagongshe.com/reaction/1522277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ReactantHCID 86721855HCID 86721855—
ProductHCID 71093037HCID 7109303719.3%

Reaction Steps

(E)-1-(4-(((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)methyl)piperidin-1-yl)-4-(3,3-difluoroazetidin-1-yl)but-2-en-1-one was prepared 5,6-dichloropyrimidin-4-amine, 4-phenoxyphenylboronic acid, tert-butyl 4-(aminomethyl)piperidine-1-carboxylate and (E)-4-(3,3-difluoroazetidin-1-yl)but-2-enoic acid with method S1, S2, S3, S4A. Yield 19.3%. 1H NMR (CD3OD) δ 8.26 (s, 1H), 7.19-7.47 (m, 9H), 6.78 (d, 1H), 6.14 (m, 1H), 4.50 (d, 1H), 4.41 (t, 3H), 4.09 (d, 1H), 3.89 (d, 1H), 3.38 (m, 2H), 3.13 (m, 1H), 2.72 (t, 1H), 1.91 (m, 1H), 1.76 (t, 2H), 1.28 (m, 2H). HPLC PURITY: 99%, MS: m/z=535[M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-a3bbab6980c341428e29e9dfc6f4d78d
Source noteuspto-grants-2015_07