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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057536Generated: November 1, 2026

N5-(2-methylpropyl)4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amine → N5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamine

https://huagongshe.com/reaction/1057536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN5-(2-methylpropyl)4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amineHCID 12015802—
ReactantSodium hydrogen sulphideHCID 86586439—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductN5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamineHCID 1201580390.8%

Reaction Steps

N5-(2-Methylpropyl)-4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amine (1.5 g, 5.22 mmol) was suspended in acetic acid (75 mL). An excess of sodium hydrogen sulfide was dissolved in a minimum of water and added to the suspension. The reaction mixture turned red and all of the material went into solution. The reaction mixture was extracted twice with dichloromethane (150 mL). The extracts were combined, washed with water, dried over magnesium sulfate, filtered and concentrated under vacuum to provide 1.22 g of N5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamine as a light yellow solid, m.p. 203-204.5° C. Analysis: Calculated for: C12H15N7: %C, 56.02; %H, 5.88; %N, 38.11; Found: %C, 55.68; %H, 5.81; %N, 37.74.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514985B1
Source datasetuspto-grants-2003_02
ORD IDord-313d6b7295ab4be1ab97682a1429ce99
Source noteuspto-grants-2003_02