HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 69584822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-Phenethylpiperazine | HCID 79214 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 22236426 | HCID 22236426 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69584822 | HCID 69584822 | — |
Reaction Steps
To a 100 mL round-bottomed flask equipped with condenser and N2 inlet were added 157 mg (0.50 mmol) 6-(4-carboxymethylnaphthalen-1-yl)-pyridin-2-ylamine, 95 mg (0.50 mmol) N-phenethylpiperazine, 96 mg (0.50 mmol) N-ethyl, N-3-dimethylaminopropyl-carbodiimide, 0.230 mL (1.65 mmol) triethylamine, 10 mg N-hydroxybenzotriazole, and 7 mL dry acetonitrile. The reaction was stirred at room temperature 12 hours (LCMS showed P+1=451 and TLC showed Rf=0.3 in 10% methanol/methylene chloride), then evaporated and the residue chromatographed on silica gel using methanol/methylene chloride as eluant to afford the product as a foam, 230 mg (˜100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07012078B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-7e87a4da94004eb1961433b23d64ae00 |
| Source note | uspto-grants-2006_03 |