HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 9950997, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Azetidine hydrochloride | HCID 12308726 | — |
| Reactant | Phenyl N-(4-(1-(methylamino)carbonyl-1H-5-indolyloxy)-2-pyridyl)-N-(phenoxycarbonyl)carbamate | HCID 21949175 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9950997 | HCID 9950997 | 61.6% |
Reaction Steps
Azetidine hydrochloride (104 mg, 1.11 mmol) and triethylamine (0.155 ml, 1.11 mmol) were added to a dimethylformamide (1 ml) solution of phenyl N-(4-(1-(methylamino)carbonyl-1H-5-indolyloxy)-2-pyridyl)-N-(phenoxycarbonyl)carbamate (116 mg, 0.222 mmol) synthesized in Production example 5-2; and the reaction mixture was stirred overnight at room temperature. The reaction mixture was partitioned between ethyl acetate and water; the organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was washed with a solvent mixture of ether-hexane=1:1; and the resultant solid was filtered off to yield the title compound (50 mg) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109219B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-fda12f6dbf2245fdb693bc6779d2b8ba |
| Source note | uspto-grants-2006_09 |