HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxaldehyde → HCID 68818603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 57593297 | HCID 57593297 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68818603 | HCID 68818603 | — |
Reaction Steps
To a solution of N-(3-((4-((3-aminopropyl)amino)-5-bromo-2-pyrimidinyl)amino)phenyl)-1-pyrrolidinecarboxamide (1.0 g, 1.97 mmol) in THF (30 mL) was added 2-thiophenecarboxaldehyde (184 mg, 1.64 mmol, 0.8 equiv.), triethylamine (362 mg, 3-6 mmol, 1.8 equiv.) and sodium triacetoxyborohydride (688 mg, 3.25 mmol, 1.6 equiv.). The resulting mixture was stirred overnight at room temperature under N2. The reaction was quenched by satuarated sodium bicarbonate (30 mL) and was extracted with ethyl acetate (3×30 mL). The reaction mixture was concentrated. Purification by HPLC chromatography using acetonitrile/water gave the title compound (310 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504410B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-58bee59f13cb4b3ea42a1a24ff3ce534 |
| Source note | uspto-grants-2009_03 |