HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 70296521, compound → HCID 54028746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 70296521 | HCID 70296521 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 54028746 | HCID 54028746 | 142.8% |
Reaction Steps
1.2 g (3.56,mmoles) of 1-(4-aminostyryl)-4-methyl-7,8-dimethoxy-3,4-dihydro-5H-2,3-benzodiazepine prepared according to Example 33 is suspended in 6 ml of acetic anhydride. The suspension is stirred for 1 hour at room temperature. In the meantime the starting compound gets dissolved, the end-product begins to separate and the reaction mixture gets thick. The separated product is filtered off, washed three times with 15 ml each of diethyl ether and dried at a temperature between 80° C. and 100° C. Thus 1.07 g (71.3%) of the desired compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075018 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-f4174ff51da241c1813447c69df03813 |
| Source note | uspto-grants-2000_06 |