HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896518Generated: October 27, 2026
Ammonium Hydroxide → 1-amino-5H-pyrido[4,3-b]indole-4-carboxamide
https://huagongshe.com/reaction/1896518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-chloro-5H-pyrido[4,3-b]indole-4-carboxamide | HCID 59198457 | — |
| Product | 1-amino-5H-pyrido[4,3-b]indole-4-carboxamide | HCID 23581927 | — |
Reaction Steps
A mixture of 1-chloro-5H-pyrido[4,3-b]indole-4-carboxamide in conc. NH4OH (0.07 M) was heated in a microwave reactor at 160° C. for 1 h in a sealed tube. The reaction mixture was cooled to room temperature and partitioned between THF/EtOAc and saturated NaHCO3. After separation of the organic phase, the aqueous phase was extracted again with THF/EtOAc, and the combined organic phases were washed with brine, dried over Na2SO4 and filtered. After evaporation of the organic solvents, the residue was purified by flash chromatography (0-10% MeOH in EtOAc) to provide the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518964B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-49b2949afb5345aeb15da52b494fad4e |
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| Source note | uspto-grants-2013_08 |
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