HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863934Generated: November 2, 2026
Hydrazine hydrate (1:1) → HCID 34176375, compound
https://huagongshe.com/reaction/1863934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-Chloro[1,2,4]triazolo[1,5-c]pyrimidine | HCID 12603817 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 34176375 | HCID 34176375 | — |
Reaction Steps
A solution of 155 mg (1 mmol) of 5-chloro[1,2,4]triazolo[1,5-c]pyrimidine [D. J. Brown and K. Shinozuka, Aust. J. Chem., 33, 1147 (1980)] in 6 mL of dry ethanol was added gradually to a vigorously stirred solution of 198 mg (204 mg, 4 mmol) of hydrazine monohydrate in 2 mL of dry ethanol. A white precipitate separated during the addition. After 1.5 h, the solid was collected on a filter. It was suspended in 2 mL of concentrated ammonium hydroxide and agitated for a few minutes. The solid was then collected on a filter and washed with some additional concentrated ammonium hydroxide, then with some ethanol, and finally with a large volume of diethyl ether. After drying, the title compound was obtained as a white solid, mp 245-246° C. (decomposition). LC-MS 151 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625888B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-7c66aa33cfc743a6a46ae284730bdea5 |
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| Source note | uspto-grants-2009_12 |
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