HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1,3-benzothiazole → N-[1-(1,3-benzothiazol-2-yl)piperidin-4-yl]-4-bromo-5-methyl-1H-pyrrole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1,3-benzothiazole | HCID 612040 | — |
| Reactant | HCID 68579819 | HCID 68579819 | — |
| Product | N-[1-(1,3-benzothiazol-2-yl)piperidin-4-yl]-4-bromo-5-methyl-1H-pyrrole-2-carboxamide | HCID 68582949 | — |
Reaction Steps
Title compound was synthesized by an analogous method to Example 123 by coupling 4-bromo-5-methyl-N-piperidin-4-yl-1H-pyrrole-2-carboxamide hydrochloride (Intermediate 57) with 2-bromo-1,3-benzothiazole (commercially available).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709503B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-43bab24f15dd4a498704f29a7c10edaa |
| Source note | uspto-grants-2010_05 |