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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367247Generated: October 31, 2026

3-Phenylpropylamine → HCID 66991236, compound

https://huagongshe.com/reaction/2367247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenylpropylamineHCID 16259—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58504757HCID 58504757—
ProductHCID 66991236HCID 6699123615.3%

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), (3-phenylpropyl)amine (500 mg, 3.70 mmol), and Hunig's base (2 mL) in 1-1-methyl-2-pyrrolidinone (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 (90 mg) as a yellow solid. LC-MS (ES) m/z=360 [M+H]+. 1H NMR (400 MHz, DMSO-d6): δ 1.80-1.87 (m, 2H), 2.64-2.68 (m, 2H), 3.28-3.30 (m, 2H), 5.37 (s, 2H), 5.97 (s, 2H), 6.27 (s, 1H), 6.93 (s, 1H), 7.17-7.31 (m, 5H), 7.40 (d, J=8.4 Hz, 1H), 7.70 (d, J=8.0 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-d4984f786fb744d5b2126f40268d5a36
Source noteuspto-grants-2014_04