HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hydroxybenzotriazole → 5-Chloro-N-[(1S)-2-[[2-[4-(4-chlorophenyl)-1-piperazinyl]-2-oxoethyl]amino]-2-oxo-1-(2-pyridylmethyl)ethyl]-1-benzofuran-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 5-Chloro-1-benzofuran-2-carboxylic acid | HCID 937838 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 69933682 | HCID 69933682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-N-[(1S)-2-[[2-[4-(4-chlorophenyl)-1-piperazinyl]-2-oxoethyl]amino]-2-oxo-1-(2-pyridylmethyl)ethyl]-1-benzofuran-2-carboxamide | HCID 9894516 | 88.5% |
Reaction Steps
To a suspension of (2S)-2-amino-N-[2-[4-(4-chlorophenyl)-1-piperazinyl]-2-oxoethyl]-3-(2-pyridyl)propanamide (18 g) and 5-chloro-1-benzofuran-2-carboxylic acid (8.8 g) in N,N-dimethyl-formamide (180 ml) were added 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (9.44 g) and N-hydroxybenzotriazole (6.66 g) at 0° C. The mixture was stirred at room temperature for 14 hours. The reaction mixture was poured into ice-cold saturated aqueous sodium hydrogencarbonate solution and the resulting solid was collected by filtration. The solid was washed successively with saturated aqueous sodium hydrogencarbonate solution and water. The solid was crystallized from water:ethanol (1:9 (v/v)) to give the title compound (23 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825200B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-db6cf40fedda4658941602b6027c89bf |
| Source note | uspto-grants-2004_11 |