HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (R)-3-[3-(piperazin-1-yl)propionyl]amino-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | 3-(1-TERT-BUTOXYCARBONYLPIPERAZIN-4-YL)PROPIONIC ACID | HCID 2735644 | — |
| Reactant | (S)-3-[3-[1-(tert-Butoxycarbonyl)piperazin-4-yl]propionyl]amino-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine | HCID 67243642 | — |
| Product | (R)-3-[3-(piperazin-1-yl)propionyl]amino-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine | HCID 57580086 | — |
Reaction Steps
(S)-3-[3-[1-(tert-Butoxycarbonyl)piperazin-4-yl]propionyl]amino-1-(4-chloro-5-isoquinolinesulfonyl)pyrrolidine can be prepared from hydrochloride of the compound prepared in Example 19-2 by using 3-[1-(tert-butoxycarbonyl)piperazin-4-yl]propionic acid in the method of Example 56-1 instead of 2-methoxyacetic acid, and the protective group of the obtained compound can be removed according to the method described in Example 1-1, Step B to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964613B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-6adc808f1aa1473b925b48a802a83961 |
| Source note | uspto-grants-2011_06 |