HuagongsheHuagongshe Chemistry Print Report · For research reference only
17beta-Carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one → 17Hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 17beta-Carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one | HCID 10002872 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 17Hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene | HCID 22881208 | — |
Reaction Steps
A solution of 17β-carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one (2.30 g, 5.33 mmol), example 1, part E, in methylene chloride (70 mL) at -78° C. is treated with diisobutylaluminum hydride (1.5M in toluene, 15 mL, 22.5 mmol). After 20 minutes the reaction is quenched with methanol (4 mL), methylene chloride added (150 mL), washed with 2N NaOH and water, dried over MgSO4 and concentrated to give crude 17hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene of sufficient purity to carry on to the following steps; yield: 2.16 g (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05708001 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-6c66fbcbf77e44e28af67cf917a3ccce |
| Source note | uspto-grants-1998_01 |