HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-piperidin-1-yl-propyl)-terephthalamic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidine-1-propylamine | HCID 19049 | — |
| Reactant | Terephthalic acid monomethylester chloride | HCID 53442854 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-piperidin-1-yl-propyl)-terephthalamic acid methyl ester | HCID 11673899 | 78% |
Reaction Steps
Triethylamine (250 mg, 2.5 mmol) and 3-piperidinopropylamine (284 mg, 2.0 mmol) are dissolved in CH2Cl2 (5 mL). Terephtalic acid monomethyl ester chloride (197 mg, 2.0 mmol) in 2.0 ml of CH2Cl2 is added to the mixture. The reaction mixture is stirred at room temperature for 2 h. The reaction is diluted with CH2Cl2 and washed with brine. The separated organic layer is dried over Na2SO4 and evaporated. The crude material is purified by silica-gel column chromatography (CH2Cl2:2M NH3 in MeOH) to give 473 mg (78%) of the title compound. MS (APCI+) 305 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008296B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-0a3e8aa707ac4276be9676d9852195ce |
| Source note | uspto-grants-2011_08 |