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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387600Generated: October 30, 2026

Dichloromethane → Hydrazine

https://huagongshe.com/reaction/2387600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHydrazineHCID 9321—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHydrazineHCID 9321—
ProductDiisopropylethylamineHCID 81531—

Reaction Steps

Alternatively, as also shown in Scheme VI, intermediate III-2 can be treated with hydrazine and an appropriate base such as triethylamine, diisopropylethylamine or excess hydrazine in a suitable organic solvent such as DCM, THF, DCE, acetone, DMF or acetonitrile to give intermediate VI-3. Intermediate VI-3 can then be treated with BrCN in the presence of a suitable base such as triethylamine, diisopropylethylamine, K2CO3, NaHCO3, or NaOAc in an appropriate organic solvent such as DCE, DCM, THF, ether, or acetonitrile at room temperature or elevated temperatures to give oxadiazole VI-4. Functionalization of the amino group affords oxadiazoles VI-5 (Arzneimittel-Forschung (2003), 53(5), 301-306; Heterocyclic Communications (2003), 9(2), 199-202; Arzneimittel-Forschung (2003), 53(1), 44-52).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268871B2
Source datasetuspto-grants-2012_09
ORD IDord-b25d3cebdf714864995abda3db739244
Source noteuspto-grants-2012_09