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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192822Generated: October 31, 2026

Pyridine → HCID 75235279, compound

https://huagongshe.com/reaction/1192822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium AzideHCID 33557—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 86681505HCID 86681505—
SolventAcetonitrileHCID 6342—
ProductHCID 75235279HCID 75235279—

Reaction Steps

At −10° C., trifluoromethanesulphonic anhydride (42 μl, 1.5 eq.) was added to a solution of 63 mg (0.16 mmol) of tert-butyl{6-[({[2-(methylamino)-2-oxo-1-phenylethylidene]amino}oxy)methyl]pyridin-2-yl}carbamate (36:64 mixture of Z and E diastereoisomers) and pyridine (53 μl, 4 eq.) in acetonitrile (1.6 ml). After warming to room temperature, the mixture was stirred for a further 1 h at 50° C. and then cooled again to room temperature. Then, 32 mg of sodium azide were added and the mixture was stirred again at 50° C. for one hour. The mixture was cooled to room temperature and a sample was analyzed using LCMS. The sample comprises 87% of the expected tert-butyl {6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate (36:64 mixture of Z and E diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680283B2
Source datasetuspto-grants-2014_03
ORD IDord-ca7cf056197241dc99e20bcd0d90e66e
Source noteuspto-grants-2014_03