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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883494Generated: November 1, 2026

2,4,6-Trimethylpyridine → HCID 54293223, compound

https://huagongshe.com/reaction/1883494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(2S)-{[(Benzyloxy)carbonyl]amino}(cyclohexyl)acetic acidHCID 16218812—
SolventDimethylformamideHCID 6228—
ProductHCID 54293223HCID 54293223—

Reaction Steps

To (S)-benzyloxycarbonylamino-cyclohexyl-acetic acid (5.4 g, 18.66 mmol) and 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (4.0 g, 18.66 mmol) in dimethylformamide were added HATU (7.09 g, 18.66 mmol) and collidine (2.46 ml, 18.66 mmol) at 0° C. The mixture was stirred for 1 hour and then allowed to warm to room temperature. The mixture was evaporated and separated between ethyl acetate and sodium bicarbonate solution. The organic layer was washed with aqueous solution (pH 4), dried and evaporated. The resulting residue was taken up in ethyl acetate and washed with potassium hydrogen sulfate solution, dried and evaporated to give the desired product. Yield: 8.29 g (91%), MS m/z: 488.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759420B1
Source datasetuspto-grants-2004_07
ORD IDord-4ef2fc6549b74c0a8e127b3eb45785f1
Source noteuspto-grants-2004_07