HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glutaric anhydride → HCID 23367636, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | HCID 23367631 | HCID 23367631 | — |
| Reactant | HCID 23367634 | HCID 23367634 | — |
| Product | HCID 23367636 | HCID 23367636 | — |
Reaction Steps
These materials were prepared using the procedures outlined in steps 2 and 3 of Example 2, except starting with 5-[4-(benzyloxycarbonyl)piperazinocarbonyl]-5H-dibenzo[b,f]azepine in place of the N-[3-(benzyloxycarbonylamino)propyl]carbamazepine in step 2, and thus the product 5-(Piperazinocarbonyl)-5H-dibenzo-[b,f]azepine Hydrobromide in place of the product of step 2, and glutaric anhydride in place of succinic anhydride in the procedures of step 3. The residue (2B) was crystallized from ethyl acetate (10 mL) and petroleum ether (2 mL), placed in a freezer, and filtered to give the acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05395933 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-ddfb9f8245274cb8adc25bb6c9fe5478 |
| Source note | uspto-grants-1995_03 |