HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227282Generated: October 26, 2026
Dicyclohexylcarbodiimide → HCID 12163872, compound
https://huagongshe.com/reaction/227282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3,4-Dichlorophenylacetic acid | HCID 79874 | — |
| Reactant | 2-(Methylamino)-1-(pyridin-3-yl)ethan-1-ol | HCID 22498734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12163872 | HCID 12163872 | — |
Reaction Steps
To a flask containing 630 mg (3.1 mmol) of DCC (dicyclohexylcarbodiimide) was added 3 ml of methylene chloride and with stirring a solution of 625 mg (3.1 mmol) of 3,4-dichlorophenyl acetic acid in 5 ml of methylene chloride was added dropwise resulting in the formation of a precipitate. The reaction mixture was stirred for 5 minutes, and to it was added 550 mg (3.05 mmol) of 1-(3-pyridyl)-2-methylaminoethanol in 6 ml of methylene chloride, it was stirred further for 1 hour at 20° C. A precipitate formed was filtered off, and the resulting solution was evaporated. The evaporated filtrate was purified by column chromatography on silica gel (silica gel 60, mobile phase: CHCl3:CH3OH=10:0.5). This yields 0.56 g (50%) of 1-(3-pyridyl)-2-(N-(2-(3,4-dichlorophenyl)acetyl)-N-propylamino)ethanol in the form the oil (molecular weight: 367.278, gross formula: C18H20N2O2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07560474B2 |
|---|
| Source dataset | uspto-grants-2009_07 |
|---|
| ORD ID | ord-3da898e69729456b8260a63820591ab2 |
|---|
| Source note | uspto-grants-2009_07 |
|---|