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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186280Generated: October 30, 2026

HCID 57701025, compound → HCID 178486007, compound

https://huagongshe.com/reaction/1186280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57701025HCID 57701025—
ReactantMethyl thiophene-2-carbimidothioate hydroiodideHCID 66704664—
SolventEthanolHCID 702—
ProductHCID 178486007HCID 17848600782.5%

Reaction Steps

To a solution of tert-butyl 3-(5-amino-1H-indol-3-yl)cyclohexyl(methyl)carbamate (0.57 g, 1.66 mmol) in dry EtOH (25 mL) was added methyl thiophene-2-carbimidothioate hydroiodide (0.75 g, 3.32 mmol) and the reaction left to stir at room temperature for 48 h. 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 (0.62 g, 81%). 1H-NMR (DMSO-d6) δ 1.35 (s, 9H), 1.42-1.71 (m, 5H), 1.88-1.93 (m, 2H), 1.98-2.04 (m, 1H), 2.69 (s, 3H), 3.40-3.53 (m, 1H), 4.24-4.27 (m, 1H), 6.22 (s, 2H, NH), 6.64 (dd, 1H, J=1.8, 8.4 Hz), 6.93 (s, 1H), 7.09 (dd, 1H, J=3.6, 5.1 Hz), 7.28 (d, 2H, J=8.4 Hz), 7.58 (d, 1H, J=4.5 Hz), 7.70 (d, 1H, J=3.6 Hz), 10.68 (s, 1H, NH); ESI-MS (m/z, %) 453 (MNa+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673909B2
Source datasetuspto-grants-2014_03
ORD IDord-98c3c82fef1941f2ba9186c2791f94da
Source noteuspto-grants-2014_03