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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458940Generated: October 29, 2026

Acetic Acid → HCID 18442427, compound

https://huagongshe.com/reaction/458940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 18442428HCID 18442428—
SolventDimethylformamideHCID 6228—
ProductHCID 18442427HCID 1844242767.6%

Reaction Steps

1,1-Dioxo-3,3-dibutyl-5-(4-aminophenyl)-8-methoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (Method 105; 918 mg, 2.13 mmol) was dissolved in DMF (dry, 20 ml). Sodium thiomethoxide (810 mg, 11.6 mmol) was added. The reaction mixture was treated at 100–120° C. for four hours then room temperature overnight. Acetic acid (3 ml) was added and the mixture was flushed with nitrogen (g) and the gas was lead through a flask containing sodium hypochlorite in order to destroy the methyl mercaptan formed. Water was added and the water layer was extracted two times with EtOAc. The combined organic layer was washed with brine, dried, filtered and evaporated under reduced pressure. The mixture contained DMF so toluene and brine was added (everything didn't dissolved). The water layer was extracted two times with toluene. The combined organic layers were washed once with brine. The separation funnel was washed with EtOAc in order to dissolve everything. The toluene and EtOAc solutions were combined, dried, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography using DCM:EtOAc, 7:3 as eluent to give the title compound 0.6 g (27%). M/z 417.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192945B2
Source datasetuspto-grants-2007_03
ORD IDord-71c72aeab44a4853a13892ac8b52120c
Source noteuspto-grants-2007_03