HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12202Generated: October 25, 2026
Methane → 6-chloro-7-ethylsulfanyl-9H-beta-carbolin-8-ylamine
https://huagongshe.com/reaction/12202
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-chloro-7-ethylsulfanyl-8-nitro-9H-beta-carboline | HCID 67165758 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-chloro-7-ethylsulfanyl-9H-beta-carbolin-8-ylamine | HCID 67166595 | 100% |
Reaction Steps
A 50 ml round-bottom flask with magnetic stirrer was charged with 6-chloro-7-ethylsulfanyl-8-nitro-9H-β-carboline (85.0 mg, 0.28 mmol) in 10 ml anhydrous ethanol. To the resulting orange mixture at RT was added 0.33 M aqueous ammonium chloride (2.0 ml, 0.66 mmol) and iron powder (680 mg, 12.2 mmol). The reaction mixture was heated to 60° C. and stirred vigorously for 20 hr. Next, the mixture was cooled to RT, diluted with ethyl acetate (15 ml), and activated charcoal (˜180 mg) was added. The resulting mixture was filtered through a pad of celite and the filtrate was concentrated to afford 77.8 mg of 6-chloro-7-ethylsulfanyl-9H-β-carbolin-8-ylamine as a yellow solid (>99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727985B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-99de42632e8e4623a5dd2ee602d10fb0 |
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| Source note | uspto-grants-2010_06 |
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