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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707977Generated: October 30, 2026

Carbon Disulfide → HCID 136118801, compound

https://huagongshe.com/reaction/1707977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 67780415HCID 67780415—
SolventMethanolHCID 887—
ProductHCID 136118801HCID 13611880120.8%

Reaction Steps

4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy) methoxy]-2-pyrimidine carboxylic acid hydrazide (0.9 g, 2.5 mmoles), KOH (0.16 g, 2.8 mmoles), and carbon disulfide (0.44 g, 5.8 mmoles) are dissolved in 20 mL of MeOH. The reaction mixture is warmed to reflux under argon for 24 hours. It is cooled to room temperature, quenched with 150 mL of 10% HOAc/H2O, and extracted with ether (3×100 mL). The ether extract is washed with brine (3×100 mL) and evaporated. The oil remaining is taken up in 20 mL of TFA and stirred at room temperature for 30 minutes. The TFA is evaporated on the rotovap, and the oil is partitioned between 100 mL of ether and 100 mL of H2O. The pH of the water layer is adjusted to 5 by the addition of saturated sodium bicarbonate. The layers are separated and the organic layer is washed with 50 mL of brine. Drying over MgSO4 and evaporation of solvent gives a yellow oil. Flash chromatography in 50% Et2O/hexane followed by two recrystallizations from Et2O/hexane gives 0.16 g (20%) of 5-[ 4,6-bis (1,1-dimethylethyl)-5-hydroxy-2-pyrimidinyl]-1,3,4-oxadiazole-2 (3H)-thione, 234°-236° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356898
Source datasetuspto-grants-1994_10
ORD IDord-290d8e0d8dc542529d41cf900801613b
Source noteuspto-grants-1994_10