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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648431Generated: October 31, 2026

Water → HCID 15281055, compound

https://huagongshe.com/reaction/1648431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 15281054HCID 15281054—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15281055HCID 1528105555%

Reaction Steps

To a stirred solution of N-(1,1-dimethylethyl)-4-azido-3-oxoandrost-4-ene-17β-carboxamide (1.3 g, 3.15 mmole) in tetrahydrofuran (20 mL)-water (7 mL) was added triphenylphosphine (1.41 g, 5.38 mmole). The reaction was heated at reflux temperature for 16 hours. Most of the tetrahydrofuran was removed under vacuum. Dichloromethane was added to the mixture and the organic solution was placed atop a column of silica gel and flash chromatographed (hexane-30% ethyl acetate). The fractions containing the product were combined and concentrated to a white solid which was crystallized from diethyl ether to give the 4-amino-N-(1,1-dimethylethyl)-3-oxoandrost-4-ene-17β-carboxamide (0.67 g, 54.9%). IR 3476, 3442, 3382, 1672, 1659, 1620(m), 1580(m) cm-1 ; MS (CI) m/z 387 (100% M+ +1); (EI) m/z 386 (10%, M+), 343 (100%); 1H NMR (CDCl3) δ 0.72 (3H, s, C18 -Me), 1.16 (s, C19 -Me), 1.34 (s, tBu-Me's), 3.49 (2H, br s, NH 2), 5.08 (1H, s, NHCO); 13C NMR (CDCl3) δ 132.97, 138.39, 171.69, 194.22. This compound has the following structure: ##STR5##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436237
Source datasetuspto-grants-1995_07
ORD IDord-325a982b9350461ebe193828bcbc206e
Source noteuspto-grants-1995_07