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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348451Generated: October 23, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 69522970, compound

https://huagongshe.com/en/reaction/348451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2,6-Dimethyl-3-pyridinolHCID 70732—
Reactant[5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl esterHCID 69522849—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 69522970HCID 6952297031.2%

Reaction Steps

A mixture of [5-(4-fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid methyl ester (prepared above, 50 mg, 0.17 mmol), 2,6-dimethyl-pyridin-3-ol (21 mg, 0.17 mmol) and DMAP (41 mg, 0.34 mmol) were slurried in dichloromethane. The solution was treated with (3-dimethylamino-propyl)-ethyl-carbodiimide (EDC) (54 mg, 0.28 mmol). After 1 h, thin layer chromatography indicated complete conversion. The reaction mixture was quenched with 10 mL 1 M HCl(aq) and 30 mL dichloromethane. The phases were partitioned, and the aqueous phase extracted with 5 mL dichloromethane. The organic phases were combined and sequentially washed with 10 mL portions of 0.1 M HCl(aq), saturated. NaHCO3(aq) and brine. The organic layer was dried using Na2SO4, filtered and concentrated. The resulting 31 mg of off-white solid was chromatographed over SiO2 (5% methanol/dichloromethane) to yield 21 mg (31%) of the titled compound. ESI-MS z/z 397 (MH+), 395 (M−H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176310B1
Source datasetuspto-grants-2007_02
ORD IDord-7c2bfd226611437088d8a1a060901427
Source noteuspto-grants-2007_02