HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → N-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | N-benzyl-4-(pyridin-2-yl)thiazol-2-amine | HCID 2902584 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amine | HCID 58614641 | — |
Reaction Steps
A solution of N-benzyl-4-(pyridin-2-yl)thiazol-2-amine (60 mg, 0.23 mmol) in DMF (2 mL) was cooled to 0° C. and treated with N-chlorosuccinimide (33 mg, 0.25 mmol), and the reaction mixture was allowed to warm to room temperature. The solvent was evaporated, and the product was purified on reverse phase HPLC to produce N-benzyl-5-chloro-4-(pyridin-2-yl)thiazol-2-amine. MS (Q1) 302.2 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888364B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-8233f7d92a354f708951ac2c74f968d1 |
| Source note | uspto-grants-2011_02 |