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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522280Generated: November 1, 2026

4-Phenoxyphenylboronic acid → HCID 71093056, compound

https://huagongshe.com/reaction/1522280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
Reactanttert-Butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylateHCID 52987765—
ReactantHCID 86721854HCID 86721854—
ProductHCID 71093056HCID 710930561.7%

Reaction Steps

(E)-1-(6-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)oxy)-2-azaspiro[3.3]heptan-2-yl)-4-(3-fluoroazetidin-1-yl)but-2-en-1-one was prepared 5,6-dichloropyrimidin-4-amine, 4-phenoxyphenylboronic acid, tert-butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylate and (E)-4-(3-fluoroazetidin-1-yl)but-2-enoic acid with method S1, S2, S3, S4A. Yield 1.7%. 1H NMR (CD3OD) δ 8.28 (s, 1H), 7.10-7.47 (m, 9H), 6.62 (m, 1H), 6.40 (t, 1H), 5.41 (m, 1H), 5.25 (m, 1H), 4.27 (d, 2H), 4.04 (m, 4H), 2.74 (m, 2H), 2.27 (m, 2H). HPLC PURITY: 99%, MS: m/z=516[M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-8e15c4308a9149cebbdb1a274d135cdf
Source noteuspto-grants-2015_07