Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284013Generated: October 30, 2026

Acetic Acid → 5-Cyclohexyl 3-methylamino 4,5,6,7-tetrahydro indazole

https://huagongshe.com/reaction/1284013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl EtherHCID 3283—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Cyclohexyl 2-methylthiocarbamoyl cyclohexanoneHCID 21515281—
SolventEthanolHCID 702—
Product5-Cyclohexyl 3-methylamino 4,5,6,7-tetrahydro indazoleHCID 21515284—

Reaction Steps

0.7 g of 4-cyclohexyl 2-methylthiocarbamoyl cyclohexanone dissolved in 30 ml ethanol are added with 0.15 g hydrazine hydrate. The mixture is heated to reflux for 30 mn until the evolution of sulphydric gas has ceased. 0.3 ml acetic acid are thereafter added and the whole is refluxed for 3 hours. The mixture is evaporated off giving a yellow liquid as residue. The residue is taken up with ether; the organic solution is washed with a saturated aqueous solution of sodium bicarbonate then with water until the washings are neutral, finally dried and evaporated off. 0.6 g of 5-cyclohexyl 3-methylamino 4,5,6,7-tetrahydroindazole are thus recovered and recrystallized from the minimum amount of isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978044
Source datasetuspto-grants-1976_08
ORD IDord-5c95b3b7eac4496dab84dc969a03bfe7
Source noteuspto-grants-1976_08