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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910173Generated: November 4, 2026

1,1-Dimethylhydrazine → HCID 67414770, compound

https://huagongshe.com/reaction/910173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DimethylhydrazineHCID 5976—
ReactantBenz-3,1-oxazine-2,4-dione, 1-pentyl-HCID 143462—
SolventTolueneHCID 1140—
ProductHCID 67414770HCID 6741477067.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

The obtained 1-pentyl-3,1-benzoxazin-2,4-(1H)-dione (0.301 g, 1.29 mmol) was dissolved in toluene (4 ml), N,N-dimethylhydrazine (0.10 ml, 1.32 mmol) was added, and the mixture was stirred at 100° C. for 2 hr. The reaction mixture was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to give N′,N′-dimethyl-2-pentylaminobenzohydrazide (0.218 g, 0.87 mmol, yield 67%). This was dissolved in methanol (3 ml), 36% formalin (0.35 ml, 4.31 mmol), sodium cyanoborohydride (0.174 g, 2.62 mmol) and acetic acid (0.1 ml) were added, and the mixture was stirred at room temperature for 20 hr. The reaction mixture was concentrated under reduced pressure, and ethyl acetate was added. The mixture was washed with water, and the organic layer was dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to give an acylhydrazine compound N′,N′-dimethyl-2-(N-methyl-N-pentylamino)benzohydrazide (0.103 g, 0.39 mmol, yield 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022072B2
Source datasetuspto-grants-2011_09
ORD IDord-08c7222b3c084a69b44c73581ee8709a
Source noteuspto-grants-2011_09