HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Acetylhydrazino)-5-(2-methylphenyl)-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,3,4-Thiadiazol-2(3H)-one, 5-(2-methylphenyl)-, hydrazone, monohydrochloride | HCID 3050131 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(2-Acetylhydrazino)-5-(2-methylphenyl)-1,3,4-thiadiazole | HCID 13684027 | — |
Reaction Steps
A solution of 2-hydrazino-5-(2-methylphenyl)-1,3,4-thiadiazole hydrochloride (1.0 g) in a mixture of acetic anhydride (0.5 ml) and pyridine (0.5 ml) was kept at room temperature under nitrogen for 0.5 hr. The solution was poured into water (100 ml) and extracted three times with methylene chloride. The organic layer was evaporated and the residue was fractionated on two 20 × 20 cm, 2 mm thick silica preparative t.l.c. plates by eluting with chloroform-methanol (4:1). The resultant product was crystallised from ethyl acetate (0.32 g; 31%) m.p. 165°-6°. C11H12N4OS requires C, 52.8; H, 5.6; N, 22.4; S, 12.8 Found C, 52.8; H, 5.1; N, 22.8; S, 13.2%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04147794 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-2c5a6dd7d1a84bc39915fb88606761fb |
| Source note | uspto-grants-1979_04 |