HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14620588, compound → HCID 14620592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14620588 | HCID 14620588 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14620592 | HCID 14620592 | 80% |
Reaction Steps
The title compound was prepared as described in Example 18 by the reduction of 5,9,15,15a-tetrahydro-3-methoxy-[1,3]dioxolo[4,5-h]isoquino-[1,2-b][3]benzazepine-8(6H)-one hemiethanolate (XIIb, Ex. 14) (3.60 g, 10 mmole) with deborane in tetrahydrofurane (25 ml of 1.0M solution). The product was extracted with methylene chloride. The methylene chloride extract was dried (Na2SO4), and evaporated on a rotary evaporator to give an oil which solidified on standing. Recrystallization from ethanol afforded the titled compound (2.57 g, 80%), mp 133°-135°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04849420 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-7450796744fd47bfacde9098ddf38c21 |
| Source note | uspto-grants-1989_07 |