Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-Bromo-3-nitropyridine | HCID 555054 | — |
| Reactant | 7-Bromo-6-azaindole | HCID 19696456 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | 1H-pyrrolo[2,3-c]pyridin-7-amine | HCID 19080186 | — |
Reaction Steps
To 84 ml of aqueous concentrated ammonia were added 600 mg (3.05 mmol) of 7-bromo-1H-pyrrolo[2,3-c]pyridine synthesized from 2-bromo-3-nitropyridine in the same manner as in Production Example 1a, 194 mg of a copper powder and 603 mg of cuprous chloride. The mixture was heated in a sealed tube at 120° C. for 15 hours and then treated, to give 170 mg of 7-amino-1H-pyrrolo[2,3-c]pyridine. The resulting product was reacted and treated in the same manner as in Examples 1a and 2a, to give 57 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834049B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-1984b068d707462f827e7c0a08a19cc2 |
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| Source note | uspto-grants-2010_11 |
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