HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 131724976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | HCID 9829761 | HCID 9829761 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131724976 | HCID 131724976 | 148.5% |
Reaction Steps
10-(5-Chloro-4-cyclohex-1-en-1-yl-2-methoxybenzoyl)-N-methyl-N-(pyridin-3-ylmethyl)-10,11-dihydro-5H-pyrrolo[2,1- c][1,4]benzodiazepine-3-carboxamide of Example 1 (0.200 g, 0.344 mmol), was dissolved in boiling diethyl ether. A solution of L-(+)-tartaric acid (0.0520 g, 0.344 mmol) in hot methanol (1 mL) was added, the mixture cooled and solvent evaporated. Diethyl ether was added to the residue causing a white solid to form which was filtered and dried in vacuo to provide 0.252 g of the title compound tartaric acid salt, m.p. 138-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903087B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-54bfaa63665740b69eb1b82ecc41c433 |
| Source note | uspto-grants-2005_06 |