Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 86676944 | HCID 86676944 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67466567 | HCID 67466567 | 73.1% |
Reaction Steps
To a suspension of 6-chloro-8-(pyridin-3-yl)imidazo[1,2-b]pyridazine (160 mg, 0.69 mmol) in EtOH (15 mL) was added ammonium formate (175 mg, 2.77 mmol) and palladium hydroxide on carbon (50 mg, 0.07 mmol) (20% wet) under nitrogen. The reaction mixture was heated to 50° C. for 20 min and cooled to room temperature. The reaction mixture was passed through a pad of CELITE® and washed with MeOH. The filtrate was concentrated and the residue was purified by BIOTAGE® (20-60% EtOAc/CH2Cl2, 1.5 L) to give the product (99 mg, 73%). LC (Condition B & C): >95% homogeneity index. LC/MS: Rt=0.31 min. LC/MS (Condition A): 197.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145419B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b680b121cb2643c0895af39aa552b435 |
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| Source note | uspto-grants-2015_09 |
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