Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 66958157 | HCID 66958157 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | HCID 66958168 | HCID 66958168 | — |
Reaction Steps
To a solution of 25 mL dioxane, 19 mL ethanol and 12 mL distilled water was added tert-butyl 4-(5-nitro-1H-indazol-3-yl)-5,6-dihydropyridine-1(2H)-carboxylate (618 mg, 1.79 mmol). To the mixture was added powdered iron (0) (502 mg, 5.0 eq) and ammonium chloride (385 mg, 4.0 eq). The reaction was heated to 70° C. under argon for 3 h. The reaction was cooled, filtered and washed with MeOH. The solvent was removed to obtain the crude which was purified by silica gel chromatography to afford the desired compound tert-butyl 4-(5-amino-1H-indazol-3-yl)-5,6-dihydropyridine-1(2H)-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501763B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-63fa06725c4840318af607a2ede5befa |
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| Source note | uspto-grants-2013_08 |
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