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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780482Generated: October 31, 2026

Dimethylformamide → HCID 54447123, compound

https://huagongshe.com/reaction/1780482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4,7-dimethyl-1,3-benzothiazoleHCID 2049879—
Reactant(+)-(4aR)-(10bR)-4-methyl-8-mercapto-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 22865069—
SolventEthyl AcetateHCID 8857—
ProductHCID 54447123HCID 5444712369.1%

Reaction Steps

A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-mercapto-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one (100 mg, 0.38 mmol), potassium carbonate (158 mg, 1.14 mmol), 2-chloro-4,7-dimethylbenzothiazole (91 mg, 0.46 mmol) and 1 mL of anhydrous dimethylformamide, fitted with a reflux condenser, and the stirred mixture was heated at 60°, under nitrogen, for 18 h. The mixture was cooled, diluted with ethyl acetate (75 mL) and washed with brine (2×25 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (80% ethyl acetate/hexanes eluent) to give 111 mg (69%) of the title compound as an amorphous foam. FDMS: m/e=422. α[D]589 =+63.27 (c=0.95, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629007
Source datasetuspto-grants-1997_05
ORD IDord-9fe0c840ecdf488ba6dd0f9d86ef1cd9
Source noteuspto-grants-1997_05