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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 21537426HCID 21537426—
ReactantN-[4-(2-Furanyl)-1,6-dihydro-5-methyl-6-oxo-2-pyrimidinyl]acetamideHCID 135762623—
ProductHCID 21537578HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957766
Source datasetuspto-grants-1976_05
ORD IDord-aca4c33174ef4fb7aa120a71aa8cae6d
Source noteuspto-grants-1976_05