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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant17beta-Carboxy-6-t-butylcarboxy-6-azaandrost-4-en-3-oneHCID 86749034—
Product17beta-N-t-butylcarbamoyl-6-t-butylcarboxy-6-azaandrost-4-en-3-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05543406
Source datasetuspto-grants-1996_08
ORD IDord-7d602a5252c644e38640bed047e42f51
Source noteuspto-grants-1996_08