HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → HCID 178520191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 4-(4-Aminophenyl)morpholin-3-one | HCID 11194854 | — |
| Reactant | [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetic acid | HCID 178525013 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178520191 | HCID 178520191 | — |
Reaction Steps
3.3 139 mg (0.445 mmol) of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetra-methyluronium tetrafluoroborate (TBTU) are added to a solution of 100 mg (0.342 mmol) of [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetic acid and 65.7 mg (0.342 mmol) of 4-(4-aminophenyl)morpholin-3-one in 2 ml of dimethylformamide (DMF), and the mixture is stirred at room temperature for 18 hours. Saturated aqueous sodium hydrogencarbonate solution is added to the reaction mixture, and the resultant precipitate is filtered off, washed with water and dried, giving 2-[2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]-N-[4-(3-oxomorpholin-4-yl)phenyl]acetamide as a brownish solid; ESI 467.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566789B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-ba1fee99328546659a91a6fb8f01aa6f |
| Source note | uspto-grants-2009_07 |