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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581716Generated: October 31, 2026

Dichloromethane → HCID 86754200, compound

https://huagongshe.com/reaction/581716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
ReactantL-ValinolHCID 640993—
ReactantHCID 15863846HCID 15863846—
ProductHCID 86754200HCID 86754200—

Reaction Steps

To a solution of 1.4 g (0.004 mole) of (3β,5β,14β,17β)-14-Amino-3-hydroxyandrostane-17-carboxylic Acid, Methyl Ester, prepared according to the procedure described in U.S. Pat. No. 4,885,280, incorporated by reference herein, in 50 ml of CH2Cl2 under N2 and stirring, 0.78 g (0.0044 mole) of 1,1'-thiocarbonyldiimidazole is added. After 2 days of stirring at ambient temperature, the solution is heated at reflux overnight and an additional 0.16 g (0.0009 mole) of 1,1'-thiocarbonyldiimidazole is added. The solution is allowed to stir further at ambient temperature for 3 days; then 2.06 g (0.02 mole) of (S)-2-amino-3-methyl-1-butanol is added to the reaction mixture. The solution is allowed to stir for another 3 days and the solvent is then removed under reduced pressure. The residue is taken up in fresh CH2Cl2, washed with H2O until the washing is neutral. After drying over MgSO4, CH2Cl2 is removed under reduced pressure to yield the crude free base. The solid is purified by flash chromatography and then converted to its hydrochloride salt by the treatment with ethanolic HCl to yield analytically pure (3β(S),5β,14β,17β)-14-Amino-14-Amino-3-[[[(l-hydroxymethyl-2-methylpropyl)amino]thioxomethyl]oxy]androstane-17-carboxylic Acid, Methyl Ester Hydrochloride Final Product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922703
Source datasetuspto-grants-1999_07
ORD IDord-f4024dd0cb5f4fd8a73d41180a968b21
Source noteuspto-grants-1999_07