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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647415Generated: October 31, 2026

Carbon Disulfide → HCID 136118801, compound

https://huagongshe.com/reaction/1647415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 67780415HCID 67780415—
SolventMethanolHCID 887—
ProductHCID 136118801HCID 13611880120%

Reaction Steps

4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidine carboxylic acid hydrazide (0.9 g, 2.5 moles), KOH (0.16 g, 2.8 moles), 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. Analysis for C14H20N4O2S: Calcd.: C, 54.52; H, 6.54; N, 18.17; S, 10.40. Found: C, 54.46; H, 6.40; N, 18.38; S, 10.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432181
Source datasetuspto-grants-1995_07
ORD IDord-3a46c5ce5fcd4d22a8e2d2fb54a0891e
Source noteuspto-grants-1995_07