HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromothiazolidine-2,4-dione → 5-(6-Methyl-pyridine-2-sulfanyl)-thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromothiazolidine-2,4-dione | HCID 3493749 | — |
| Reactant | HCID 178425945 | HCID 178425945 | — |
| Product | 5-(6-Methyl-pyridine-2-sulfanyl)-thiazolidine-2,4-dione | HCID 10657687 | — |
Reaction Steps
This compound was prepared from 5-bromo-thiazolidine-2,4-dione and 2-methyl-6-mercaptopyridine (A. D. Dunn, R. Norfie, J. L'Hostis,and S. Marjot J.Prak. Chem.-Chem. Zt. 1992, 334, 119-125) according to the procedure described in Example 1: mp 114-115.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05605918 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-6928497e971f40379ee168a37d6ccf96 |
| Source note | uspto-grants-1997_02 |