HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076661Generated: November 4, 2026
Hydrazine hydrate (1:1) → HCID 21537578, compound
https://huagongshe.com/reaction/1076661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21537426 | HCID 21537426 | — |
| Reactant | N-[4-(2-Furanyl)-1,6-dihydro-5-methyl-6-oxo-2-pyrimidinyl]acetamide | HCID 135762623 | — |
| Product | HCID 21537578 | HCID 21537578 | — |
Reaction Steps
1-methyl-2-[2,8-dimethyl-7-(5-nitro-2-furyl)-s-triazolo[2,3-c]pyrimidinyl-5-]-imino-pyrrolidine (m.p. 244° - 246°C.) from the N-methyl-pyrrolidone-(2)-phosphorus oxychloride adduct and 2,8-dimethyl-5-amino-7-(5-nitro-2-furyl)-s-triazolo[2,3-c]pyrimidine; the latter compound (m.p. 290° - 295°C.) used as starting material was obtained by chlorinating 2-acetamido-4-(2-furyl)-5-methyl-6(1H)-pyrimidinone and the intermediate obtained (m.p. 155° - 160°C.) reacted with hydrazine hydrate to give 2-amino-4-(2-furyl)-6-hydrazino-5-methyl-pyrimidine (m.p. 220° - 222°C.) which was cyclised with orthoacetic acid triethyl ester, the intermediate obtained then nitrated to give 5-amino3,8-dimethyl-7-(5-nitro-2-furyl)-s-triazolo[4,3-c]pyrimidine (m.p. 290°C.; decomp.) which was heated in ethanol saturated with hydrogen chloride;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957766 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-aca4c33174ef4fb7aa120a71aa8cae6d |
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| Source note | uspto-grants-1976_05 |
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