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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118230Generated: October 31, 2026

4-Methylmorpholine → HCID 178483788, compound

https://huagongshe.com/reaction/2118230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 178484857HCID 178484857—
SolventDichloromethaneHCID 6344—
ProductHCID 178483788HCID 17848378882.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

120 mg (0.29 mmol) of trans-3-{4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-propionic acid in 3 mL of CH2Cl2 were treated with 0.057 mL (0.44 mmol, 1.5 eq) of N,N,N′-trimethylethylenediamine and 0.48 mL (0.36 mmol, 1.5 eq) of NMM. The solution was cooled to 0° C. and 73.0 mg (0.38 mmol, 1.3 eq) of EDCI and 9 mg (0.06 mmol, 0.2 eq) of HOBT were added. The mixture was stirred at RT for 2 days, partitioned between CH2Cl2 and a saturated aqueous solution of NaHCO3. The organic phase was washed with brine, dried over Na2SO4 and evaporated. Column chromatography with CH2Cl2:MeOH 9:1 gave 118 mg (82%) of trans-N-(2-dimethylamino-ethyl)-N-methyl-3-{4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-propionamide as colorless oil, MS: 494 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442791B2
Source datasetuspto-grants-2008_10
ORD IDord-be91c7718f25456ab72d108557bdb504
Source noteuspto-grants-2008_10