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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264101Generated: October 30, 2026

Water → (3beta,5beta,7alpha,12alpha)-3-(9H-Fluoren-9-ylmethoxy)amino-7,12-dihydroxycholan-24-oic acid

https://huagongshe.com/reaction/2264101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
Reactant3beta-amino-7alpha,12alpha-dihydroxy-5beta-cholan-24-oic AcidHCID 54018831—
SolventSodium CarbonateHCID 10340—
Solvent1,4-DioxaneHCID 31275—
Product(3beta,5beta,7alpha,12alpha)-3-(9H-Fluoren-9-ylmethoxy)amino-7,12-dihydroxycholan-24-oic acidHCID 8659542571%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 9-fluorenylmethoxycarbonyl chloride (1.4 g; 5.4 mmol) in 1,4-dioxane (18 mL) was added dropwise to a suspension of (3β,5β,7α,12α)-3-amino-7,12-dihydroxycholan-24-oic acid A (2.0 g; 4.9 mmol) (3) in 10% aq. Na2CO3 (30 mL) and 1,4-dioxane (18 mL) stirred at 0° C. After 6 h stirring at room temperature H2O (100 mL) was added, the aqueous phase washed with Et2O (2×90 mL) and then 2 M HCl (15 mL) was added (final pH: 1.5). The precipitated solid was filtered, washed with H2O (3×100 mL), vacuum dried and then purified by flash chromatography to give B as a white solid (2.2 g; 3.5 mmol). Yield 71%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07850947B2
Source datasetuspto-grants-2010_12
ORD IDord-e559f21210934a90850df0d303acb3eb
Source noteuspto-grants-2010_12