HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178523843, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-indole-2-carbonyl Chloride | HCID 11816208 | — |
| Reactant | HCID 178479292 | HCID 178479292 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178523843 | HCID 178523843 | — |
Reaction Steps
On the other hand, to a suspension of (3S)-3-amino-1,3-dihydro-5-phenyl-1-[(1H-tetrazol-5-yl) methyl]-2H-1,4-benzodiazepin-2-one hydrochloride in dry dichloromethane (50 ml) was added dropwise triethylamine (7.45 ml). To the mixture was added dropwise a solution of 2-indolylcarbonyl chloride obtained above under stirring and cooling below 10° C. After stirring under the same conditions for 2 hours, the mixture was washed with hydrochloric acid, water and brine. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethanol to give (3S)-1,3-dihydro-3-(2-indolylcarbonylamino)-5-phenyl-1-[(1 H-tetrazol-5-yl)-methyl]-2H-1,4-benzodiazepin-2-one (5.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264433 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-98635ecd8f5044e39321797167f2cd1f |
| Source note | uspto-grants-1993_11 |