HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 137629483, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 140511257 | HCID 140511257 | — |
| Product | HCID 137629483 | HCID 137629483 | 20% |
Reaction Steps
To ethyl 5-bromo-4-(bromomethyl)-2-{[(2-imino-4-oxo-1,3-thiazolidin-5-yl) acetyl]amino}thiophene-3-carboxylate (25 mg, 0.05 mmol) in N,N dimethyl formaide (1 mL) was added aniline (10 mg, 0.11 mmol). The reaction mixture was stirred at room temperature for 16 h. Then the reaction mixture was concentrated and purified by reverse phase column to yield ethyl 4-(anilinomethyl)-5-bromo-2-{[(2-imino-4-oxo-1,3-thiazolidin-5-yl)acetyl]amino}thiophene-3-carboxylate (5.0 mg, 20% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563813B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-2d659069f990454aad4d7e65f23349e7 |
| Source note | uspto-grants-2009_07 |