HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11706086, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-[2-(3,5-Difluoro-phenyl)-acetylamino]-pentanoic acid | HCID 21942986 | — |
| Reactant | HCID 68834228 | HCID 68834228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11706086 | HCID 11706086 | — |
Reaction Steps
A mixture of 2-[2-(3,5-difluoro-phenyl)-acetylamino]-pentanoic acid (25.4 mg, 0.2 mmol), 5-(2-phenyl-propylsulfanyl)-[1,3,4]thiadiazol-2-ylamine (50 mg, 0.2 mmol), HBOT (29 mg, 0.21 mmol), EDC HCl (46 mg, 0.24 mmol.) and triethylamine (0.12 ml) in methylene chloride was stirred at room temperature until product formation or disappearance of starting material. The mixture was quenched with water and extracted with methylene chloride. The organic layer was separated, washed with dilute HCl, brine, dried over sodium sulfate and the solvent was removed at reduced pressure to provide the title compound as a cude oil. The oil was purified by Shimadzu HPLC to provide the title compound as a light yellow solid (26 mg), LC-MS M+1=505.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253195B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-7b5ef962107245809ef22689f56927e3 |
| Source note | uspto-grants-2007_08 |