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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925558Generated: October 28, 2026

Isoamylamine → 2-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]-sulfanyl]-N-(3-methyl-butyl)-pyridine-3-carboxylic acid amide

https://huagongshe.com/reaction/1925558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-(3,3-Difluoro-3-(4-fluorophenyl)propylthio)-nicotinic acidHCID 67133674—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
Product2-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]-sulfanyl]-N-(3-methyl-butyl)-pyridine-3-carboxylic acid amideHCID 5948730155%

Reaction Conditions

Temperature0 °C

Reaction Steps

320 μl (1.83 mmol) of DIPEA and 350 mg (0.91 mmol) of HATU were added at 0° C. to a solution of 150 mg (0.46 mmol) of 2-(3,3-difluoro-3-(4-fluorophenyl)propylthio)-nicotinic acid in DCM (10 ml). After stirring for 30 min at 0° C., 63 μl (0.55 mmol) of 3-methylbutan-1-amine were added and then the mixture was stirred for 16 h at RT. Dilution with water (20 ml) and extraction with DCM (2×20 ml) were then carried out. The combined organic phases were washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. CC (EA/hexane 7:3) of the residue yielded 100 mg (0.25 mmol, 55%) of 2-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]-sulfanyl]-N-(3-methyl-butyl)-pyridine-3-carboxylic acid amide. MS: m/z 397.1 [m+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178684B2
Source datasetuspto-grants-2012_05
ORD IDord-881e027f58c043c8a96d145817bc6702
Source noteuspto-grants-2012_05