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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036896Generated: November 2, 2026

1,2-Dichloroethane → HCID 86656599, compound

https://huagongshe.com/reaction/2036896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(Dimethylamino)butyric acid hydrochlorideHCID 12691640—
ReactantHCID 86656618HCID 86656618—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 86656599HCID 86656599—

Reaction Steps

A mixture of 200 mg N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide, 67 mg 4-dimethylaminobutyric acid hydrochloride, 111 mg HOBt, 276 mg EDC, 0.603 ml triethylamine and 7 ml DMF is stirred overnight. The reaction mixture is quenched with 3 ml water and 5 ml dichloromethane. The organic phase is separated, the water phase extracted twice with dichloromethane. The combined organic phases are dried and evaporated. 280 ml of a yellow oil is obtained, which is further purified by preparative HPLC-methods.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575193B2
Source datasetuspto-grants-2013_11
ORD IDord-a0957707bc63488097d353e1eddfce8f
Source noteuspto-grants-2013_11