HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077590Generated: November 1, 2026
Tert-Butylamine → 17beta-N-t-butylcarbamoyl-6-t-butylcarboxy-6-azaandrost-4-en-3-one
https://huagongshe.com/reaction/1077590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 17beta-Carboxy-6-t-butylcarboxy-6-azaandrost-4-en-3-one | HCID 86749034 | — |
| Product | 17beta-N-t-butylcarbamoyl-6-t-butylcarboxy-6-azaandrost-4-en-3-one | HCID 86749705 | — |
Reaction Steps
A sample of 17β-carboxy-6-t-butylcarboxy-6-azaandrost-4-en-3-one (2.03 g, 4.86 mmol), from part F, is coupled with t-butyl amine as described in Example 1, part A, to give crude 17β-N-t-butylcarbamoyl-6-t-butylcarboxy-6-azaandrost-4-en-3-one which is dissolved in methylene chloride (30 mL) and treated with trifluoroacetic acid (4 mL) at room temperature. After 3 hrs the reaction is concentrated, methylene chloride (50 mL) and saturated aqueous bicarbonate (50 mL) added, the layers separated, methylene chloride washed with saturated aqueous NaCl, dried over MgSO4, concentrated and chromatographed on silica gel (0-10% methanol/methylene chloride) to give 17β-N-t-butylcarbamoyl-6-azaandrost-4-en-3-one as a white solid; yield: 1.04 g (57%). Recrystallization from methylene chloride/hexanes gives an analytical sample as a white crystalline solid; m.p. 186°-189° C. Anal. Calcd. for C23H36N2O2 ·3/8H2O; C, 72.83; H, 9.77; N, 7.38. Found C, 72.95; H, 9.85; N, 7.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05543406 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-7d602a5252c644e38640bed047e42f51 |
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| Source note | uspto-grants-1996_08 |
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