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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522208Generated: November 4, 2026

Acryloyl chloride → HCID 86721806, compound

https://huagongshe.com/reaction/1522208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
ReactantTert-butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylateHCID 25212937—
ProductHCID 86721806HCID 86721806—

Reaction Steps

1-(1-((6-amino-5-(4-phenoxyphenyl)pyrimidin-4-yl)amino)-7-azaspiro[3.5]nonan-7-yl)prop-2-en-1-one was prepared from 5,6-dichloropyrimidin-4-amine, tert-butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylate, (4-phenoxyphenyl)boronic acid and acryloyl chloride according to general scheme 3 using methods S1, S2, S3, and S4C. HPLC purity: 99%. MS: m/z=456 [M+H]+. 1H NMR (CD3OD) δ 8.24 (s, 1H), 7.11-7.50 (m, 9H), 6.73 (m, 1H), 6.18 (d, 1H), 5.71 (d, 1H), 4.53 (m, 1H), 4.21 (m, 1H), 3.83 (m, 1H), 3.18 (m, 1H), 2.95 (m, 1H), 2.27 (m, 2H), 2.06 (m, 1H), 1.86 (m, 2H), 1.68 (m, 3H), 1.37 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073947B2
Source datasetuspto-grants-2015_07
ORD IDord-714386828468457bbf31c20e1526c407
Source noteuspto-grants-2015_07