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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713434Generated: November 1, 2026

Dichloromethane → Hydrazine

https://huagongshe.com/reaction/1713434

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 numberUS07795282B2
Source datasetuspto-grants-2010_09
ORD IDord-f8855d0cb92240e898b2a00ddf6da333
Source noteuspto-grants-2010_09