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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845972Generated: October 30, 2026

Hydrochloric Acid → HCID 71008676, compound

https://huagongshe.com/reaction/1845972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-Methylcyclopropane-1-sulfonamideHCID 21889814—
ReactantHCID 71008354HCID 71008354—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 71008676HCID 7100867647%

Reaction Conditions

Temperature40 °C

Reaction Steps

The product of Example 1f, (2R,6S,13aS,14aR,16aS,Z)-2-(3-fluorophenanthridin-6-yloxy)-6-(5-methylisoxazole-3-carboxamido)-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a-carboxylic acid (0.812 g, 1.21 mmol) was dissolved in dichloroethane (12 mL) and 4A sieves were added to the flask. To this mixture was added carbonyldiimidazole (505 mg, 3.11 mmol) and the reaction mixture was heated at 40° C. for 2 h. The reaction mixture was cooled to room temperature and 1-methylcyclopropane-1-sulfonamide (426 mg, 3.15 mmol) was added followed by 1,8-diazabicycloundecene (0.548 ml, 3.64 mmol). The reaction mixture was stirred at room temperature for 3 h. and then cooled to 0° C. and 4 N HCl in dioxane (2.5 mL, 10 mmol) was added. The resulting solid was washed copiously with dichloromethane and the filtrate was washed with 2 N HCl and then water. The organic layer was dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with acetone/hexane followed by acetone/chloroform to provide the title compound (0.45 g, 47% yield) as a white solid. MS (ESI): m/z=787.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951964B2
Source datasetuspto-grants-2015_02
ORD IDord-39bd383f66bd4158a98664784d0f30cc
Source noteuspto-grants-2015_02