HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910173Generated: November 4, 2026
1,1-Dimethylhydrazine → HCID 67414770, compound
https://huagongshe.com/reaction/910173
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dimethylhydrazine | HCID 5976 | — |
| Reactant | Benz-3,1-oxazine-2,4-dione, 1-pentyl- | HCID 143462 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67414770 | HCID 67414770 | 67.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022072B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-08c7222b3c084a69b44c73581ee8709a |
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| Source note | uspto-grants-2011_09 |
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