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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581713Generated: October 30, 2026

Dichloromethane → Hydrochloric Acid

https://huagongshe.com/reaction/581713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 15863846HCID 15863846—
ProductHydrochloric AcidHCID 313—
ProductHCID 131721300HCID 131721300—

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, is added 0.72 g (0.0044 mole) of 1,1'-carbonyldiimidazole. The mixture is allowed to stir for 2 days, then 2.24 g (0.02 mole) of N,N-diethylethylenediamine is added. After 48 hr of stirring, the solution is concentrated and the residue is taken up with fresh CH2Cl2 and is washed well with water until the washing is neutral. After drying over MgSO4, CH2Cl2 is removed under reduced pressure to yield 1.55 g of crude free base. Purification via flash chromatography using 3% MeOH/CH2Cl2 (NH4OH) at first, followed by 4% and then 7% MeOH/CH2Cl2 provides the free base. Treatment with ethanolic HCl yields the analytically pure (3β,5β,14β,17β)-14-Amino-3-[[[[2-(diethylamino)ethyl]amino]carbonyl]oxy]androstane-17-carboxylic Acid, Methyl Ester Dihydrochloride Final Product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922703
Source datasetuspto-grants-1999_07
ORD IDord-3df8cc3846d94578a24cff9f42c2853b
Source noteuspto-grants-1999_07