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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750362Generated: October 31, 2026

N-Methylpyridine-4-methylamine → HCID 86721200, compound

https://huagongshe.com/reaction/1750362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methylpyridine-4-methylamineHCID 81436—
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-(2-(1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetic acidHCID 86721182—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86721200HCID 8672120065%

Reaction Steps

A solution of 2-(2-(1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetic acid (60 mg, 0.17 mmol), HATU (76 mg, 0.20 mmol), DIEA (0.035 mL, 0.20 mmol) and N-methyl-1-(pyridin-4-yl)methanamine (20.39 mg, 0.17 mmol) in DMF (1 mL) was stirred at room temperature for 2 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by NH-silica gel column chromatography (solvent gradient; 5→80% ethyl acetate/hexane) to give the title compound (50 mg, 0.108 mmol, 65%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-bed5d39043e7488f98c5cd02b9f29a43
Source noteuspto-grants-2015_10