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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772362Generated: November 3, 2026

Toluene → HCID 178435021, compound

https://huagongshe.com/reaction/1772362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantHydrazineHCID 9321—
ReactantLawesson's reagentHCID 87949—
Reactant(1S,2R)-5'-(4-chlorophenyl)-2,6',7'-trimethylspiro[cyclopropane-1,3'-thieno[2,3-e][1,4]diazepin]-2'(1'H)-oneHCID 136338068—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178435021HCID 17843502182.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

A round bottomed flask was charged with (1S,2R)-5′-(4-chlorophenyl)-2,6′,7′-trimethylspiro[cyclopropane-1,3′-thieno[2,3-e][1,4]diazepin]-2′(1′H)-one (289 mg, 0.838 mmol) and a stir bar. Toluene (8.5 mL, 0.1 M) added, followed by Lawesson's Reagent (186 mg, 0.461 mmol), and the reaction was stirred at 110° C. After conversion to the thioamide intermediate, as determined by LC/MS, the reaction was cooled and diluted with THF (20 mL) for the addition of hydrazine (263 μl, 8.38 mmol). The reaction was stirred at room temperature before being concentrated and purified by column chromatography to give (1S,2R)-5′-(4-chlorophenyl)-2′-hydrazono-2,6′,7′-trimethyl-1′,2′-dihydrospiro[cyclopropane-1,3′-thieno[2,3-e][1,4]diazepine] (249 mg). LRMS (M+H)+: 359 m/z

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249161B2
Source datasetuspto-grants-2016_02
ORD IDord-d792863bd3c2438288de8c0ae79a35a2
Source noteuspto-grants-2016_02