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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725133Generated: November 1, 2026

[6-(3-Amino-prop-1-ynyl)-quinazolin-4-yl]-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenyl]-amine → HCID 178426750, compound

https://huagongshe.com/reaction/1725133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[6-(3-Amino-prop-1-ynyl)-quinazolin-4-yl]-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenyl]-amineHCID 66623351—
ReactantHCID 178512385HCID 178512385—
SolventIsopropanolHCID 3776—
ProductHCID 178426750HCID 17842675051.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 2-phenyl-N-cyano-isourea (50 mg, 0.31 mmol) and [6-(3-amino-prop-1-ynyl)-quinazolin-4-yl]-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenyl]-amine (30 mg, 0.076 mmol) in isopropanol (3 mL) was heated at 85° C. in a sealed tube. The reaction was cooled to room temperature after 5 hours. Solvent was removed via rotovap. The residue was then purified by FCC to give the final product (18 mg, 51%) as a light yellow solid. MS ESI (+) m/z 463 (M+1) detected; 1H NMR (400 MHz, deuterated DMSO) □ 9.9 (s, 1H), 8.7 (s, 1H), 8.6 (s, 1H), 8.2 (s, 1H), 7.8 (m, 2H), 7.75 (m, 2H), 7.2 (m, 3H), 7.0 (m, 3H), 4.22 (m, 2H), 2.42 (s, 3H), 2.2 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488823B2
Source datasetuspto-grants-2009_02
ORD IDord-b9ae1ef8b2eb49d58d75e75e44b42f39
Source noteuspto-grants-2009_02