Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 67926897 | HCID 67926897 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53749054 | HCID 53749054 | — |
Reaction Steps
3-Carbomethoxy-3-androstene-17β-carboxylic acid, (360 mg, 0.78 mmol) was suspended in 10 ml of dry toluene and treated with 0.4 ml of oxalyl chloride for 2 hours under argon. The reaction mixture was then evaporated (1 mm Hg) and the residue was dissolved in 10 ml dry THF. A solution of 0.6 ml diisopropylamine in 2 ml dry THF was added and the reaction mixture stirred for 1 hour. The mixture was diluted with ice water and extracted with dichlorome thane. The organic layer was then washed twice with cold 5% hydrochloric acid, sodium hydroxide and brine; dried over sodium sulfate and evaporated. Chromatography on silica gel eluting with 20% ethyl acetate in hexane followed by recrystallization from diethyl ether afforded 3-carbomethoxy-3-androstene 178 N,N -diisopropylcarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017568 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-97e1ed1a60b64e04bde80fd6be91e67f |
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| Source note | uspto-grants-1991_05 |
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