HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21881058, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 21881060 | HCID 21881060 | — |
| Reactant | HCID 21881063 | HCID 21881063 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21881058 | HCID 21881058 | — |
Reaction Steps
A solution of PMB-CB-OH (1.154 g, 2.881 mmol), 15-maleinimido-4,7,10,13-tetroxapentadecanoic acid (1.49 g, 4.32 mmol) and triethylamine (1.20 ml, 8.64 mmol) in 20 ml anhydrous dichloromethane is admixed with 2-chloro-1-methylpyridinium iodide (1.10 g, 4.32 mmol) and stirred for three hours at room temperature. It is diluted with 80 ml dichloromethane, washed each time twice with 50 ml 1 n hydrochloric acid, 50 ml water and once with 50 ml sodium chloride solution (saturated) and dried over magnesium sulfate. Subsequently the solvent is removed in a vacuum and the residue is purified by column chromatography (silica gel, ethyl acetate). 1.93 g PMB-CB-4-Mal (92% of theory) is obtained as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141691B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-225e558d85db4fe5a48a8a59d5cc9972 |
| Source note | uspto-grants-2006_11 |