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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265882Generated: October 30, 2026

1,2-Dichloroethane → HCID 86619629, compound

https://huagongshe.com/reaction/2265882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
ReactantHCID 66879432HCID 66879432—
SolventDimethylformamideHCID 6228—
ProductHCID 86619629HCID 8661962980%

Reaction Steps

A solution of 40 mg (0.264 mmol) of HOBt and 51 mg (0.264 mmol) of EDC in 2 ml of DMF was added dropwise to a solution of 98 mg (0.176 mmol) of 2-[4-(4-fluoro-phenoxy)benzenesulfonyl]-6-(2-morpholin-4-ylethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid and 46 mg (0.325 mmol) of O-(tetrahydropyran-2-yl)hydroxylamine in 3 ml of DMF at 0° C., and the mixture was stirred at room temperature. After standing overnight, it was poured onto H2O and extracted with ethyl acetate. The organic phase was dried with MgSO4 and concentrated. The residue was chromatographed on silica gel (dichloromethane→dichloromethane/methanol 99:1), the title compound being isolated as a colorless solid. Yield: 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858619B2
Source datasetuspto-grants-2010_12
ORD IDord-5f8f62975af7437f9e82c9dcc9253875
Source noteuspto-grants-2010_12