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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405480Generated: November 1, 2026

2-Pyridineethanamine → HCID 67776389, compound

https://huagongshe.com/reaction/2405480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridineethanamineHCID 75919—
ReactantHCID 86666173HCID 86666173—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 67776389HCID 6777638970%

Reaction Steps

To a flask containing methyl 4-((1S,3aS,5aR,5bR,7aS,9S,11aS,11bR,13aR,13bR)-3a-(chlorocarbonyl)-1-isopropyl-5a,5b,8,8,11a-pentamethylicosahydro-1H-cyclopenta[a]chrysen-9-yl)benzoate (77 mg, 0.13 mmol) in DCE (2 mL) was added Hunig'sBase (0.068 mL, 0.390 mmol), DMAP (1 mg, 8.19 μmol), and 2-(2-Aminoethyl)pyridine (0.031 mL, 0.260 mmol). The mixture was stirred for 2.5 hours at rt. The reaction was diluted with 5 mL of water and was extracted with dichloromethane (3×5 mL). The combined organic layers were dried with Na2SO4. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by Biotage flash chromatography using a 0-75% ethyl acetate in hexanes gradient. The fractions containing the expected product were combined and concentrated. The expected product, methyl 4-((1S,3aS,5aR,5bR,7aS,9S,11aS,11bR,13aR,13bR)-1-isopropyl-5a,5b,8,8,11a-pentamethyl-3a-(2-(pyridin-2-yl)ethylcarbamoyl)icosahydro-1H-cyclopenta[a]chrysen-9-yl)benzoate (0.062 g, 0.091 mmol, 70.0% yield), was isolated as a white foam. LCMS: m/e 679.7 (M−H)−, 3.09 min (method 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802661B2
Source datasetuspto-grants-2014_08
ORD IDord-b9b1a0af55e24516806c7db688b706ed
Source noteuspto-grants-2014_08