HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 86619556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 11629090 | HCID 11629090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86619556 | HCID 86619556 | — |
Reaction Steps
0.5 g of (R)-1-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-2-[4-(4-methyl-piperazin-1-yl)-piperidin-1-yl]-2-oxo-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate (chemical purity: 85%, 0.59 mmol) are dissolved in 5 ml of ethanol at ambient temperature and combined with 235 μl hydrobromic acid (30% in glacial acetic acid), whereupon a white precipitate is immediately formed. The suspension is stirred for 5 hours at ambient temperature, diluted with a little ethanol and filtered. The isolated solid is dried for 12 hours at 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638625B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-c0a83f957aa746dca729c06bae08e089 |
| Source note | uspto-grants-2009_12 |