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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829622Generated: October 30, 2026

Triethylamine → HCID 10108897, compound

https://huagongshe.com/reaction/1829622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,6-dichloro-N-phenyl-1,3,5-triazin-2-amineHCID 16766—
Reactant1,4-Benzodioxan-6-ylamineHCID 89148—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10108897HCID 1010889769%

Reaction Steps

To a solution of 4,6-dichloro-N-phenyl-[1,3,5]triazine-2-amine (95 mg, 0.39 mmoles) in tetrahydrofuran (2 ml) was added a solution of 1,4-benzodioxan-6-amine (64 mg, 0.42 mmoles) and triethylamine (0.07 ml, 0.50 mmoles) in tetrahydrofuran (0.5 ml). After stirring for 24 hours, the mixture was concentrated under vacuum and the residue was dissolved in ethyl acetate (10 ml). The solution was washed with a solution composed of saturated aqueous sodium chloride solution and 1 M hydrochloric acid (1:1, 2×10 ml), dried over sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by flash chromatography on silica gel eluting with 25% ethyl acetate-hexanes to provide CT-32028 (97 mg, 69% yield). 1H NMR (d6-DMSO) δ 9.88–10.28 (m, 2 H), 7.60–7.85 (m, 2 H), 7.20–7.40 (m, 3 H), 6.96–7.10 (m, 2 H), 6.77–6.81 (m, 1 H), 4.21 (s, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064125B2
Source datasetuspto-grants-2006_06
ORD IDord-66d5aeda8dbc425e8d919a0dee88c30b
Source noteuspto-grants-2006_06