HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244133Generated: October 26, 2026
Hydrazine → 6-(Aminomethyl)-1,2,4-triazin-5(4H)-one
https://huagongshe.com/reaction/244133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-(5-Oxo-4,5-dihydro-[1,2,4]triazin-6-ylmethyl)isoindole-1,3-dione | HCID 136017966 | — |
| Solvent | Dichloromethane ethanol | HCID 21584144 | — |
| Product | 6-(Aminomethyl)-1,2,4-triazin-5(4H)-one | HCID 135742495 | — |
Reaction Steps
A slurry of 2-(5-oxo-4,5-dihydro-[1,2,4]triazin-6-ylmethyl)-isoindole-1,3-dione (4 g, 15.6 mmol) in DCM/EtOH (1:1) (150 mL) was charged with anhydrous hydrazine (1.23 mL, 39.0 mmol) and stirred at rt for 18 h. The reaction mixture was concentrated in vacuo and the off-white solid was triturated with warm CHCl3 and filtered through a fritted funnel. The solid was then triturated with hot boiling methanol (MeOH) and filtered through a fritted funnel resulting in an off-white solid. The material was triturated a second time as before and dried overnight resulting in the title compound as a white solid, which was taken on to the next step without further purification; 1H NMR (DMSO-d6, 400 MHz) δ 3.88 (s, 2H), 8.31 (2, 1H); MS (ES+): m/z 127.07 (100) [MH+], HPLC: tR=0.34 min (MicromassZQ, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653268B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-78ae303d30664a6396a40c4dc1d358ad |
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| Source note | uspto-grants-2014_02 |
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