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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604106Generated: November 1, 2026

17-Cyclopropyloxy-4-nitroandrost-4-en-3-one → 4-Amino-17-cyclopropyloxyandrost-4-en-3-one

https://huagongshe.com/reaction/1604106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17-Cyclopropyloxy-4-nitroandrost-4-en-3-oneHCID 53944425—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product4-Amino-17-cyclopropyloxyandrost-4-en-3-oneHCID 1534100164.1%

Reaction Steps

A solution of 17-cyclopropyloxy-4-nitroandrost-4-en-3-one (1.0 g, 2.71 mM) in acetic acid (10 mL) is treated with zinc dust (1.0 g). The combination is vigorously stirred for 1.5 hours at room temperature. The zinc salts are removed by filtration and washed with ethyl acetate. The combined filtrate and wash are combined and concentrated to a yellow solid which is then redissolved in ethyl acetate and extracted three times with 1M hydrochloric acid (150 ml). The combined acid extracts are neutralized with sodium hydroxide (pH 14) and further extracted with ether. The combined organic layers are then dried over sodium sulfate and concentrated to give 4-amino-17-cyclopropyloxyandrost-4-en-3-one (0.59 g), m.p. 100-102° C. (aqueous methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990328
Source datasetuspto-grants-1999_11
ORD IDord-9aeea94ee50f438d8fc130119f6388c4
Source noteuspto-grants-1999_11