HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 178486434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | HCID 57642334 | HCID 57642334 | — |
| Product | HCID 178486434 | HCID 178486434 | — |
Reaction Steps
5-(2-chlorophenyl)-1,2-dihydro-7-cyano-8-methoxy-pyrazolo[3,4-b][1,4]benzodiazepine (XXIIb) was prepared by reacting 0.00096 moles of 5-(2-chlorophenyl)-7-cyano-1,3-dihydro-8-methoxy-2H-1,4-benzodiazepin-2-thione (IIb) with 1,1-diethoxy-N,N-dimethyl-methanamine and then hydrazine in a manner analogous to the example above. Recrystallization from ethyl acetate provided 5-(2-chlorophenyl)-1,2-dihydro-7-cyano-8-methoxy-pyrazolo[3,4-b][1,4]benzodiazepine (XXIIb) as a light red solid, mp 288-290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524840B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-f1ee5258e83244799bc30c528cebf3c1 |
| Source note | uspto-grants-2009_04 |