HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → HCID 178486426, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 1-Allyl-5-chloro-3-methyl-1H-pyrazol-4-amine | HCID 57642344 | — |
| Reactant | (2-Amino-4-chloro-5-methoxyphenyl)(2-chlorophenyl)-methanone | HCID 57642385 | — |
| Reactant | HCID 178456647 | HCID 178456647 | — |
| Product | HCID 178486426 | HCID 178486426 | — |
Reaction Steps
8-chloro-5-(2-chlorophenyl)-1,2-dihydro-7-methoxy-3-methyl-pyrazolo[3,4-b][1,4]benzodiazepine (IVy) was prepared by reacting 0.0012 moles of (2-amino-4-chloro-5-methoxyphenyl)(2-chlorophenyl)-methanone (Xy) with 4-amino-5-chloro-3-methyl-1-(2-propenyl)-1H-pyrazole (XIII), and subsequent dealkylation of the intermediate, 8-chloro-5-(2-chlorophenyl)-1,2-dihydro-7-methoxy-3-methyl-1-(2-propenyl)-pyrazolo[3,4-b][1,4]benzodiazepine (XIVy) with diisobutylaluminum hydride in a manner analogous to Example 72. MH+/Z=373.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524840B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-cb7852de0c2d47698f8ce15e8e7ff10f |
| Source note | uspto-grants-2009_04 |