HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylpiperazine-1-carbothioamide → 3-[2-(4-Methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylpiperazine-1-carbothioamide | HCID 2113086 | — |
| Reactant | 3-(Bromoacetyl)benzoic acid | HCID 2756835 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[2-(4-Methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acid | HCID 58256980 | — |
Reaction Steps
4-Methyl-piperazine-1-carbothioic acid amide (2.47 mmol) and 3-(2-Bromo-acetyl)-benzoic acid (2.47 mmol) were mixed in THF (12 mL). After stirring at room temperature for 5 minutes the mixture was heated to 80° C. for 2 hours. The mixture was then cooled to room temperature and filtered. The solid was washed with a small amount of diethylether and dried. m/z=304.1 in MS ES+, which was characterized by hplc and MS and used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915300B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-fc3c537173884a8282b26ffd820a6db2 |
| Source note | uspto-grants-2011_03 |