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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458932Generated: October 29, 2026

Sodium methanethiolate → HCID 18442425, compound

https://huagongshe.com/reaction/458932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 18442424HCID 18442424—
SolventDimethylformamideHCID 6228—
ProductHCID 18442425HCID 1844242596.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192945B2
Source datasetuspto-grants-2007_03
ORD IDord-e541f018ef104de19759536392d3093d
Source noteuspto-grants-2007_03