HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-5-nitrobenzenecarbothioamide → HCID 22049688, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-5-nitrobenzenecarbothioamide | HCID 22049716 | — |
| Reactant | 2-Bromo-1-(4-methylpyridin-3-yl)ethan-1-one | HCID 22049783 | — |
| Product | HCID 22049688 | HCID 22049688 | — |
Reaction Steps
By the reaction in the same manner as in Example 25-ii) using 2-methyl-5-nitrobenzonitrile (1.25 g), 2-methyl-5-nitrobenzenecarbothioamide was obtained as a yellow powder. Then, by the reaction in the same manner as in Example 25-iii) using 2-bromo-1-(4-methylpyridin-3-yl)ethanone hydrobromate (1.35 g) and 2-methyl-5-nitrobenzenecarbothioamide, the title compound (460 mg) was obtained as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067537B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-fa360708756542308c95bf395d23f218 |
| Source note | uspto-grants-2006_06 |