Carbon Disulfide → 5-[3,5-bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]phenyl]-1,3,4-thiadiazole-2(3H)-thione

HRID 466042Notes

Reaction equation

HRID 466042 reaction equation
[C:1](=[S:3])=[S:2].[CH3:4][C:5]([C:8]1[CH:9]=[C:10]([C:25]([NH:27][NH2:28])=N)[CH:11]=[C:12]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:13]=1[O:14][CH2:15][O:16][CH2:17][CH2:18][O:19][CH3:20])([CH3:7])[CH3:6]>C(O)C.C(OC(C)C)(C)C>[CH3:7][C:5]([C:8]1[CH:9]=[C:10]([C:25]2[S:2][C:1](=[S:3])[NH:28][N:27]=2)[CH:11]=[C:12]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:13]=1[O:14][CH2:15][O:16][CH2:17][CH2:18][O:19][CH3:20])([CH3:4])[CH3:6]

Participants

5

Procedure

Carbon disulfide (1.6 g, 0 021 mole) is added dropwise to a stirred 0° C. solution of 3,5-bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzene carboximidic acid hydrazide (3.0 g, 0.085 mole) in absolute ethanol (36 ml). The mixture is allowed to warm to room temperature and stir three hours. The mixture is stripped of volatiles under reduced pressure and the residue is dissolved in isopropyl ether and the solvent removed under reduced pressure. The resulting solid is recrystallized from isopropyl ether/hexane to give 2.8 g of 5-[3,5-bis(1,1-dimethylethyl)- 4-[(2-methoxyethoxy)methoxy]phenyl]-1,3,4-thiadiazole-2(3H)-thione (3.5 g theor., 80%); mp 134°-135° C.

Workup

  1. customthe solvent removed under reduced pressure
  2. customThe resulting solid is recrystallized from isopropyl ether/hexane

Sources & evidence

ORD record
ord-0326ef7de0854a5c87b070b4ca33bb3d
Source dataset
uspto-grants-1992_10
Patent number
US05155122

Reaction notes

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