HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Benzothiazolediamine → N-(2-Amino-benzthiazol-6-yl)-2-(4-benzyl-piperidin-1-yl)-2-oxo-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Benzothiazolediamine | HCID 21504 | — |
| Reactant | (4-Benzylpiperidin-1-yl)oxoacetic acid | HCID 16110264 | — |
| Product | N-(2-Amino-benzthiazol-6-yl)-2-(4-benzyl-piperidin-1-yl)-2-oxo-acetamide | HCID 86593927 | — |
Reaction Steps
The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and 2,6-diamino-benzthiazole [Arch. Pharm., 13, 48. (1935)] according to the method described in Example 2. The filtered crystals are purified by column chromatography using Kieselgel 60 (Merck) as adsorbent and toluene:methanol=4:1 as eluent. Melting Point: 203° C. (isopropanol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435744B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-c680c423911c4a609026f78c7472d0b5 |
| Source note | uspto-grants-2008_10 |