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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574213Generated: October 30, 2026

3-Amino-6-bromo-5-(trifluoromethyl)picolinohydrazide → 2-(5-(1,1,1-Trifluoro-2-(triisopropylsilyloxy)propan-2-yl)-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyridin-3-amine

https://huagongshe.com/reaction/574213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-6-bromo-5-(trifluoromethyl)picolinohydrazideHCID 86729595—
Reactant6-Bromo-2-(5-(1,1,1-trifluoro-2-(triisopropylsilyloxy)propan-2-yl)-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyridin-3-amineHCID 86729598—
Reactant3-Amino-5-(trifluoromethyl)picolinohydrazideHCID 86729601—
Product2-(5-(1,1,1-Trifluoro-2-(triisopropylsilyloxy)propan-2-yl)-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyridin-3-amineHCID 86729600—

Reaction Steps

The title compound was prepared analogously to 6-bromo-2-(5-(1,1,1-trifluoro-2-(triisopropylsilyloxy)propan-2-yl)-1,3,4-oxadiazol-2-yl)-5-(trifluoromethyl)pyridin-3-amine (Example 10, step 3) by replacing 3-amino-6-bromo-5-(trifluoromethyl)picolinohydrazide (Intermediate H) (step 1) with 3-amino-5-(trifluoromethyl)picolinohydrazide (Int. I); LCMS: Rt=1.66 min; [M+H]+ 499.3 Method 2minLC_v003.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034879B2
Source datasetuspto-grants-2015_05
ORD IDord-593c3fb0886543dda573bd6972f2a9cc
Source noteuspto-grants-2015_05