HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloro-2-benzothiazolamine → HCID 12093897, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloro-2-benzothiazolamine | HCID 7226 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ammonium 2-[[1-(4-pyridinyl)piperidin-4-ylmethyl]amino]pyridine-3-carboxylate | HCID 11174879 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12093897 | HCID 12093897 | 11.1% |
Reaction Steps
A solution of ammonium 2-[[1-(4-pyridinyl)piperidin-4-ylmethyl]amino]pyridine-3-carboxylate (400 mg, 1.28 mmol) in methylene chloride (5 mL) was treated with thionyl chloride (0.112 mL, 1.54 mmol) and the mixture was heated at reflux. After 3 h, the mixture was cooled and then treated dropwise with a solution of 2-amino-6-chlorobenzothiazole (284 mg, 1.54 mmol) in pyridine (5 mL). After 1 h, the mixture was concentrated in the presence of silica gel. The residue was purified by column chromatography (SiO2: 1 to 4% [2 N ammonia in methanol]:chloroform) followed by recrystallization from methanol to yield 68 mg (11%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06689780B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-6a7e3735d29a4c47bb1dbd91ec3431ee |
| Source note | uspto-grants-2004_02 |