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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367249Generated: October 30, 2026

2-Methoxyphenethylamine → HCID 66991174, compound

https://huagongshe.com/reaction/2367249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyphenethylamineHCID 74896—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58504757HCID 58504757—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 66991174HCID 6699117416.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 6-[2-amino-6-(methylsulfonyl)-4-pyrimidinyl]-1H-indazol-3-amine (500 mg, 1.64 mmol), 2-[2-(methyloxy)phenyl]ethanamine (500 mg, 3.31 mmol), and Hunig's base (2 mL) in NMP (3 mL) was heated for 4 hours at 140° C. in a BiotageInitiator® microwave synthesizer. Upon cooling, the mixture was decanted to remove the solids, and the resulting solution was concentrated to dryness. The crude material was purified by RPHPLC (gradient: 10% CH3CN/H2O to 30% CH3CN/H2O) to afford the title compound (100 mg) as a yellow solid. LC-MS (ES) m/z=376 [M+H]+. 1H NMR (400 MHz, DMSO-d6): δ 2.81-2.84 (m, 2H), 3.52 (m, 2H), 3.74 (s, 3H), 5.37 (s, 2H), 6.01 (s, 2H), 6.28 (s, 1H), 6.76-6.86 (m, 4H), 7.22 (t, J=8.4 Hz, 1H), 7.41 (d, J=7.6 Hz, 1H), 7.69 (d, J=8.8 Hz, 1H), 7.84 (s, 1H), 11.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-a9bab1ddec01444980db7e442345b9be
Source noteuspto-grants-2014_04