Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-Chlorofuro[3,2-c]pyridine | HCID 2779746 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Product | Furo[3,2-c]pyridin-4-amine | HCID 22665882 | 95% |
Reaction Steps
65.3 g (425 mmol) 4-chlorofuro[3,2-c]pyridine [CAS Reg.-No. 31270-80-1] were suspended in 600 ml aqueous ammonia solution (35%) in an autoclave. After addition of 2 g copper(I)-chloride, the reaction mixture was stirred for 20 h at 150° C. After cooling to rt, the mixture was extracted with dichloromethane (3×400 ml). The combined organic phases were washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield 46.6 g (82% of th.) of crude title compound (content >95% by GC) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604028B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-872275196f884867be503781014fef37 |
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| Source note | uspto-grants-2013_12 |
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