HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-(3-amino-4-thienyl)-N'-(4-methyl-3-thienyl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,4-Diaminothiophene dihydrochloride | HCID 12707342 | — |
| Reactant | 3-Isothiocyanato-4-methylthiophene | HCID 22139827 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-amino-4-thienyl)-N'-(4-methyl-3-thienyl)thiourea | HCID 86037734 | — |
Reaction Steps
A mixture of 1.87 g of 3,4-diaminothiophene dihydrochloride, 60 ml of anhydrous tetrahydrofuran (THF) and 2.58 g of N-ethyl-N,N-diisopropylamine was stirred at room temperature for 30 minutes and then admixed with 1.5 g of 4-methyl-3-thienyl isothiocyanate. After stirring over approx. 18 hours, the solvent was distilled off, the residue admixed with water and extracted repeatedly with ethyl acetate. After the combined organic phases had been treated with activated carbon, they were dried over sodium sulfate and the solvent was once again distilled off. The N-(3-amino-4-thienyl)-N′-(4-methyl-3-thienyl)thiourea was obtained as an amorphous foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179830B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-b42dad8b0c4d4bada62dd01825bed579 |
| Source note | uspto-grants-2007_02 |