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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470759Generated: November 3, 2026

N-Methylpyridine-4-methylamine → (S)-2-{4-[4-(1-Acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acid methyl-pyridin-4-ylmethyl-amide

https://huagongshe.com/reaction/1470759

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—
Reactant(S)-2-{4-[4-(1-Acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acidHCID 67125410—
SolventDimethylformamideHCID 6228—
Product(S)-2-{4-[4-(1-Acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acid methyl-pyridin-4-ylmethyl-amideHCID 67970548—

Reaction Steps

To 36.8 mg (0.1 mmol) (S)-2-{4-[4-(1-acetylamino-ethyl)-phenyl]-piperidin-1-yl}-pyrimidine-5-carboxylic acid (XVII.1) and 51 μL (0.3 mmol) DIPEA in 2 mL DMF is added 38.0 mg (0.1 mmol) HATU and the mixture is stirred for 15 min at rt. Subsequent the mixture is added to 12.2 mg (0.1 mmol) methylpyridin-4-ylmethylamine and stirring is continued for 12 h. The solvent is removed in vacuo and the residue is purified using reversed phase column chromatography (water+0.1% NH4OH/MeOH) and the corresponding fractions are concentrated to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006450B2
Source datasetuspto-grants-2015_04
ORD IDord-a4bbc9ad9dbd4e39b5b9219a2f5b706b
Source noteuspto-grants-2015_04