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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353956Generated: October 30, 2026

1,2-Dichloroethane → 1-Methylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/353956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylformamideHCID 6228—
Reactant4-MethylmorpholineHCID 7972—
ReactantMorpholine-4-carboxylic acid [1-(4-cyano-piperidin-4-ylcarbamoyl)-2-cyclohexyl-ethyl]-amide hydrochlorideHCID 22260409—
SolventSodium BicarbonateHCID 516892—
Product1-Methylpiperidine-4-carboxylic acidHCID 2736939—
ProductMorpholine-4-carboxylic acid {1-[4-cyano-1-(1-methyl-piperidine-4-carbonyl)-piperidin-4-ylcarbamoyl]-2-cyclohexyl-ethyl}-amideHCID 22260560—

Reaction Steps

A solution of 1-methyl-piperidin-4-yl carboxylic acid (0.050 g, 0.30 mmol, 1.0 equiv) and EDC (0.057 g, 0.30 mmol, 1.0 equiv) was prepared in 15 mL of DMF. After 15 min morpholine-4-carboxylic acid [1-(4-cyano-piperidin-4-ylcarbamoyl)-2-cyclohexyl-ethyl]-amide hydrochloride (0.128 g, 0.30 mmol, 1.0 equiv) was added followed by N-methyl-morpholine (0.12 g, 1.2 mmol, 4.0 equiv) followed by stirring overnight (16 h). The reaction mixture was diluted with 100 mL of saturated sodium bicarbonate solution and the product was extracted with 2×50 mL of EtOAc. The combined organic extracts were concentrated. The crude product was purified by semi-prep reverse-phase HPLC using 20 to 80% CH3CN in water over a gradient of 25 min to yield the desired product as a white solid (39 mg); MS, m/z 517=M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756372B2
Source datasetuspto-grants-2004_06
ORD IDord-2cbcbb9d85d54456bd765894155f0dee
Source noteuspto-grants-2004_06