HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043521Generated: October 31, 2026
3-(4-(Dimethylamino)cyclohex-1-enyl)-1H-indol-5-amine → HCID 178482648, compound
https://huagongshe.com/reaction/2043521
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-(Dimethylamino)cyclohex-1-enyl)-1H-indol-5-amine | HCID 57474460 | — |
| Reactant | Methyl thiophene-2-carbimidothioate hydroiodide | HCID 66704664 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178482648 | HCID 178482648 | 93.5% |
Reaction Steps
A solution of compound 113 (0.18 g, 0.704 mmol) in dry ethanol (10 mL) was treated with thiophene-2-carboximidothioic acid methyl ester hydroiodide (0.4 g, 1.409 mmol) at room temperature and stirred for 24 h. Solvent was evaporated and crude was diluted with sat. NaHCO3 solution (20 mL) and product was extracted into CH2Cl2 (2×25 mL). The combined CH2Cl2 layer was washed with brine (20 mL) and dried (Na2SO4). Solvent was evaporated and crude was purified by column chromatography (2 M NH3 in methanol: CH2Cl2, 1:9) to obtain compound 114 (0.24 g, 90%) as a solid. mp 113-115° C.; 1H NMR (DMSO-d6) δ 1.42-1.53 (m, 1H), 1.97-2.02 (m, 1H), 2.08-2.22 (m, 8H), 2.31-2.60 (m, 3H), 6.03 (s, 1H), 6.21 (brs, 2H), 6.65 (dd, 1H, J=1.2, 8.4 Hz), 7.09 (t, 1H, J=4.2 Hz), 7.20 (s, 1H), 7.28-7.31 (m, 2H), 7.58 (d, 1H, J=4.5 Hz), 7.71 (d, 1H, J=2.7 Hz), 10.88 (s, 1H); ESI-MS m/z (%): 365 (MH+, 39), 320 (38), 183 (76), 160 (100); ESI-HRMS calculated for C21H25N4S (MH+), Calculated: 365.1813; Observed: 365.1794.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586620B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-e14e8f6da12a4b70a2bdf053ac911f97 |
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| Source note | uspto-grants-2013_11 |
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