HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458932Generated: October 29, 2026
Sodium methanethiolate → HCID 18442425, compound
https://huagongshe.com/reaction/458932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | HCID 18442424 | HCID 18442424 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18442425 | HCID 18442425 | 96.4% |
Reaction Steps
Sodium methanethiolate (0.43 g, 6.08 mmol) was added to a solution of 1,1-dioxo-3,3-dibutyl-4-oxo-5-(4-chlorophenyl)-7-bromo-8-methoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (Method 96; 0.66 g, 1.22 mmol) in anhydrous DMF (11 ml) under nitrogen. The reaction mixture was stirred at room temperature for 72 hours. The solvent was evaporated under reduced pressure and the residue was extracted with trichloromethane/water. The organic layer was separated, washed with brine, dried and evaporated under reduced pressure. The crude product was purified by column chromatography using DCM as eluent to give the title compound 0.6 g (96%). NMR (500 MHz) 0.80–1.0 (m, 6H), 1.10–1.6 (m, 10H), 1.70–2.0 (m, 2H), 2.28 (s, 3H), 3.37–3.70 (m, 2H), 4.04 (s, 3H), 6.65 (s, 1H), 7.25–7.30 (m, 2H), 7.35–7.42 (m, 3H); m/z 510.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192945B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-e541f018ef104de19759536392d3093d |
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| Source note | uspto-grants-2007_03 |
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