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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695265Generated: October 30, 2026

4-Chloro-2-(2-chloro-acetylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester → HCID 11589947, compound

https://huagongshe.com/reaction/1695265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(2-chloro-acetylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl esterHCID 11633641—
ReactantHCID 11669941HCID 11669941—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11589947HCID 115899472%
ProductHCID 11669941HCID 116699411%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(2-Acetoxy-acetylamino)-4-chloro-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester (B) Sodium acetate (0.054 g, 0.658 mmol) in water (5 mL) was added to solution of compound of Example 4 (0.18 g, 0.405 mmol) in DMF (5 mL) at 25° C. and then the reaction mixture was stirred at 80° C. for 6 h. The solvent was removed under vacuum, water (15 mL) was added and extracted using ethyl acetate (3×30 mL). Combined organic layer was washed with water (2×100 mL), brine (100 mL) and dried over anhydrous sodium sulfate. The solvent was removed under vacuum and crude product was purified by column chromatography (silica gel) to obtain the title compound (B) (1% methanol in chloroform) and compound (A) (2% methanol in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163730B2
Source datasetuspto-grants-2012_04
ORD IDord-c9181241a5334e118e4fd57842d51090
Source noteuspto-grants-2012_04