HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 178477737, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethanesulfonic acid | HCID 11668 | — |
| Reactant | DW-1350 | HCID 178432563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178477737 | HCID 178477737 | 86% |
Reaction Steps
3 g (6.614 mmol) of N-hydroxy-4-{5-[4-(5-isopropyl-2-methyl-1,3-thiazol-4-yl)phenoxy]pentoxy}benzamidine was dissolved in 30 ml of ethanol, and was mixed with 1.14 ml (2.2 equivalents) of ethanesulfonic acid with agitation at room temperature for 1 hr. The solution was then mixed with 30 ml of acetone and 60 ml of hexane with agitation for 1 hr. The produced solid was recovered by filtration, washed with acetone, and dried under vacuum. As a result, 4.17 g (yield: 86%) of N-Hydroxy-4-{5-[4-(5-isopropyl-2-methyl-1,3-thiazol-4-yl)phenoxy]pentoxy}benzamidine 2 ethansulfonic acid salt was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039635B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-704ddf50658f40e9a3add45c8412c00b |
| Source note | uspto-grants-2011_10 |