HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Methyl-1H-indol-2-yl)boronic acid → 4-Methyl-piperazine-1-sulfonic acid 5-(1-methyl-1H-indol-2-yl)-pyridin-3-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Methyl-1H-indol-2-yl)boronic acid | HCID 22733820 | — |
| Reactant | 4-Methyl-piperazine-1-sulfonic acid 5-bromo-pyridin-3-yl ester | HCID 58215823 | — |
| Product | 4-Methyl-piperazine-1-sulfonic acid 5-(1-methyl-1H-indol-2-yl)-pyridin-3-yl ester | HCID 58215611 | — |
Reaction Steps
4-Methyl-piperazine-1-sulfonic acid 5-bromo-pyridin-3-yl ester and N-methyl-indoleboronic acid are processed according to the method described in Example 100 to give 4-Methyl-piperazine-1-sulfonic acid 5-(1-methyl-1H-indol-2-yl)-pyridin-3-yl ester. MS (ESI) m/z 387.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242963B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-49277683696146438f37a5dbc813b72e |
| Source note | uspto-grants-2016_01 |