HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazine → {2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophen-6-yl}-morpholin-4-ylmethanone tri-hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazine | HCID 17750945 | — |
| Reactant | 2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride | HCID 68858808 | — |
| Reactant | [2-(2,5-Dichloropyrimidin-4-yl)-benzo[b]thiophen-6-yl]-morpholin-4-yl-methanone | HCID 86625368 | — |
| Product | {2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophen-6-yl}-morpholin-4-ylmethanone tri-hydrochloride | HCID 68854855 | — |
Reaction Steps
Using the method of 2-[5-chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride, the title compound is synthesized from [2-(2,5-dichloropyrimidin-4-yl)-benzo[b]thiophen-6-yl]-morpholin-4-yl-methanone and 4-(3-aminopropyl)-piperazine-1-carboxylic acid tert-butyl ester and isolated as a yellow solid. ES+(m/z) 501 (35Cl) and 503 (37Cl) [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547691B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-fc216141a5134b5ba6052f6eb1e5cce7 |
| Source note | uspto-grants-2009_06 |