Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Formyl-5-methoxybenzoic acid | HCID 7176205 | — |
| Reactant | HCID 67994528 | HCID 67994528 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67994837 | HCID 67994837 | — |
Reaction Steps
A mixture of 7-acetyl-1-(3-amino-2-methylphenyl)-5H-pyridazino[4,5-b]indole-4-carboxamide (0.250 g, crude product from the previous step), 2-formyl-5-methoxybenzoic acid (0.251 g, 1.391 mmol), sodium triacetoxyborohydride (0.442 g, 2.087 mmol), and acetic acid (0.100 mL, 1.739 mmol) in dichloromethane (18 mL) and tetrahydrofuran (18 mL) was stirred at room temperature for 3 hr. Additional sodium triacetoxyborohydride (0.442 g, 2.087 mmol) was added and the reaction mixture was stirred at rt. Three hours later, another portion of sodium triacetoxyborohydride (0.442 g, 2.087 mmol) was added, and the mixture was stirred at room temperature overnight. The reaction was quenched with water (30 mL) and the mixture was extracted with ethyl acetate (4×40 mL). The combined extract was dried over anhydrous MgSO4. Removal of solvent under vacuum provided the crude desired product (0.336 g) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685969B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a5196cdb585a4dcaac5c3f1a10411c5b |
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| Source note | uspto-grants-2014_04 |
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