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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350216Generated: November 1, 2026

N-tert-butylsulfamoyl chloride → tert-butyl(3R)-3-[3-({[(tert-butylamino)sulfonyl]amino}methyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoate

https://huagongshe.com/reaction/1350216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-tert-butylsulfamoyl chlorideHCID 12682606—
Reactanttert-butyl(3R)-3-[3-(aminomethyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoateHCID 16747946—
SolventPyridineHCID 1049—
Producttert-butyl(3R)-3-[3-({[(tert-butylamino)sulfonyl]amino}methyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoateHCID 60077597—

Reaction Steps

Method as for preparation 10 using tert-butyl(3R)-3-[3-(aminomethyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoate (preparation 18) (200 mg, 0.57 mmol) and N-tert-butylsulfamoyl chloride (J. Org. Chem.; 1976, 41, 4028) (108 mg, 0.63 mmol) as starting materials and pyridine as base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214694B2
Source datasetuspto-grants-2007_05
ORD IDord-0557e89aa7944e69bfa84f4281e71251
Source noteuspto-grants-2007_05