Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830181Generated: November 4, 2026

1,2-Dichloroethane → HCID 22054100, compound

https://huagongshe.com/reaction/1830181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyric acidHCID 22053987—
ReactantHCID 86611138HCID 86611138—
SolventDichloromethaneHCID 6344—
ProductHCID 22054100HCID 22054100107.9%

Reaction Steps

To a stirred mixture of 4-morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyric acid (177 mg, 0.5 mmol), 2-amino-1-(5-phenyl-[1,3,4]oxadiazol-2-yl)-1-butanol TFA salt (175 mg), prepared as in reference 16, and HOBt (92 mg, 0.6 mmol) in MeCl2 (5 ml), was added EDC (144 mg, 0.75 mmol) and N-methylmorpholine (0.35 ml) at room temperature. After stirring for 14 hours, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated NaHCO3, brine, dried with MgSO4 and concentrated to yield 308 mg of N-{1-[Hydroxy-(5-phenyl-[1,3,4]oxadiazol-2-yl)-methyl]-propyl}-4-morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyramide. Without further purification, the crude product was used for next reaction; MS: 569.6(M−1), 571.4(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064123B1
Source datasetuspto-grants-2006_06
ORD IDord-26eaeb7dfba545b4bc5a0d48e243a3a0
Source noteuspto-grants-2006_06