HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579431Generated: November 3, 2026
Methanesulfonyl chloride → HCID 54503523, compound
https://huagongshe.com/reaction/1579431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 68131678 | HCID 68131678 | — |
| Reactant | HCID 86732878 | HCID 86732878 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54503523 | HCID 54503523 | — |
Reaction Steps
Conversion of 6α,7α-dihydroxy-4-androstene-3,17-dione to the corresponding 6α,7α-dimethanesulfonate ester by treatment with methanesulfonyl chloride in pyridine in a manner similar to that described in Example 22B followed by treatment of the resulting 6α,7α-dimethanesulfonyloxy-4-androstene-3,17-dione with sodium azide in dimethylformamide in a manner similar to that described in above Example 22C does not yield an identifiable amount of 6-azido-4,6-androstadiene-3,17-dione. Similarly, treatment of 6α,7α-dimethanesulfonyloxy-4-androstene-3,17-dione with sodium azide in aqueous methanol in the presence of acetic acid in a manner similar to that described in Example 6, does not yield an identifiable quantity of 6-azido-4,6-androstadiene-3,17-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931167 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-f28b1ce9c28e40e09007514742cc68a3 |
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| Source note | uspto-grants-1976_01 |
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