HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-(3-Methoxyphenyl)benzimidazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Amino-3'-methoxy[1,1'-biphenyl]-3-carboxylic acid | HCID 22325335 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(3-Methoxyphenyl)benzimidazolidin-2-one | HCID 22325327 | — |
Reaction Steps
To a suspension of 5-(3-methoxyphenyl)-2-aminobenzoic acid (2.0g) in 1,4-dioxane (20 mL) add N-methylpyrolidinone (NMP, 5 mL) and triethylamine (1.4 mL), followed by diphenyl phosphoric azide (DPPA, 2.5 g). After stirring at ambient temperature for 30 minutes, heat the mixture to 100° C. for 2 hours, until gas evolution fully subsided. Cool the mixture to ambient temperature and concentrate in vacuo. Dissolve the residue in MeOH and leave to stand for 18 hours. Filter the precipitate and air dry to obtain 5-(3-methoxyphenyl)benzimidazolidin-2-one as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566367B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-8b709cc66827410b9b2df21321afb77d |
| Source note | uspto-grants-2003_05 |