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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692482Generated: November 1, 2026

1,2-Dichloroethane → HCID 75070613, compound

https://huagongshe.com/reaction/1692482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCyclopropanesulfonamideHCID 15765418—
ReactantHCID 66871229HCID 66871229—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 75070613HCID 7507061339%

Reaction Steps

A solution of 17-[2-(6-isopropyl-2-pyridyl)-7-methoxy-8-methylquinolin-4-yloxy]-13-methyl-2,14-dioxo-3,13-diazatricyclo[13.3.0.04,6]octadec-7-ene-4-carboxylic acid (113, 200 mg, 0.31 mmol), DMAP (76.5 mg, 0.62 mmol), and EDC (151 mg, 0.78 mmol) in DMF (5 mL) was stirred at room temperature overnight (the activation of the acid was monitored by LC-MS). Then, cyclopropylsulfonamide (191 mg, 1.56 mmol) was added, followed by DBU (228 μL, 1.56 mmol). The resulting solution was stirred overnight at room temperature, then neutralized with acetic acid and evaporated. The residue was re-dissolved in MeOH and purified by preparative HPLC to give 90 mg (39%) of the title compound 114: m/z=744 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153800B2
Source datasetuspto-grants-2012_04
ORD IDord-baf4b4f3e1f34cafafdd268704e1a99e
Source noteuspto-grants-2012_04