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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910606Generated: October 29, 2026

HCID 66910124, compound → HCID 66910127, compound

https://huagongshe.com/reaction/910606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66910124HCID 66910124—
ReactantHCID 66910132HCID 66910132—
ReactantHCID 66910174HCID 66910174—
ProductHCID 66910127HCID 6691012775%

Reaction Steps

6-Azaandrostane-3,7,17-trione was prepared from 3β-hydroxy-6-azaandrostane-7,17-dione by the procedure described above for the preparation of 3β,17β-di(dimethyltert-butylsilyloxy)androstane-6-one and 3α,17β-di(dimethyltert-butylsilyloxy)androstane-6-one (Prepn. 12). The mixture was stirred for 35 minutes, then SiO2 was added and evaporated to dryness. The mixture was purified by flash chromatography (SiO2, acetone/toluene 1/1) to give 6-azaandrostane-3,7,17-trione (75%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 7.34 (s, 1H), 3.31 (dd, 1H), 2.57-1.07 (m, 17H), 0.99 (s, 3H), 0.83 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022203B2
Source datasetuspto-grants-2011_09
ORD IDord-659d52931fb94b01b0443396b89c96bd
Source noteuspto-grants-2011_09