HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186283Generated: October 31, 2026
HCID 57701032, compound → HCID 178465427, compound
https://huagongshe.com/reaction/1186283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57701032 | HCID 57701032 | — |
| Reactant | Methyl thiophene-2-carbimidothioate hydroiodide | HCID 66704664 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178465427 | HCID 178465427 | 99.1% |
Reaction Steps
To a solution of tert-butyl 3-(5-amino-1H-indol-3-yl)cyclohexyl(ethyl)carbamate (0.62 g, 1.73 mmol) in dry EtOH (25 mL) was added methyl thiophene-2-carbimidothioate hydroiodide (1.00 g, 3.47 mmol) and the reaction left to stir at room temperature for 48 hours. The solvent then was evaporated and the mixture dissolved in dichloromethane (20 mL) and washed with 2N NaOH (10 mL). The organic layer was extracted and evaporated. The crude was purified on column chromatography (2 M NH3 in MeOH:CH2Cl2, 2:98 to 5:95) to give the title compound as a yellow solid (0.80 g, quantitative). 1H-NMR (DMSO-d6) δ 1.04 (t, 3H, J=6.9 Hz), 1.36 (s, 9H), 1.44-1.68 (m, 5H), 1.84-2.04 (m, 3H), 3.05-3.20 (m, 2H), 3.42-3.53 (m, 1H), 4.19-4.26 (m, 1H), 6.21 (s, 2H), 6.64 (dd, 1H, J=1.8, 8.4 Hz), 6.92 (s, 1H), 7.09 (dd, 1H, J=3.6, 5.1 Hz), 7.26 (s, 1H), 7.29 (s, 1H), 7.58 (d, 1H, J=5.1 Hz), 7.70 (d, 1H, J=3.9 Hz), 10.67 (s, 1H). ESI-MS (m/z, %) 467 (MH+, 100)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673909B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-94e2e0b4d3434ff58108fe7fecc08e11 |
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| Source note | uspto-grants-2014_03 |
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