HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroethyl bromide → 2-(2-{3-[1-(2-Fluoroethyl)-piperidin-4-yl]-propylamino}-5-methyl-pyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamide di-hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | 2-[5-Methyl-2-(3-piperidin-4-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide | HCID 68854784 | — |
| Reactant | HCID 68857364 | HCID 68857364 | — |
| Product | 2-(2-{3-[1-(2-Fluoroethyl)-piperidin-4-yl]-propylamino}-5-methyl-pyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamide di-hydrochloride | HCID 86625378 | — |
Reaction Steps
Using the method of 2-{5-chloro-2-[2-(1-ethylpiperidin-4-yl)-ethylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid cyclopropylamide di-hydrochloride, the title compound is synthesized from 2-[5-methyl-2-(3-piperidin-4-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide and 1-bromo-2-fluoroethane and isolated as a yellow solid. ES+(m/z) 496 [M(free base)+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547691B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-acda8f8dd8354dd5a7a947dde36f8d32 |
| Source note | uspto-grants-2009_06 |