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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53070Generated: November 2, 2026

4-Methylmorpholine → N-(N-(N-(N-((1,1-dimethyl)ethoxycarbonyl)-L-alanyl)-L-alanyl)-L-prolyl)-L-valine [9alpha-fluoro-11beta,21-dihydroxy-16beta-methyl-3,20-dioxo-17-valeroyloxy-pregna-1,4-dien-21-yl] ester

https://huagongshe.com/reaction/53070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-ala-ala-pro-OHHCID 11902955—
Reactant(2S)-2-Amino-3-methyl-butyric acid [11beta,21-dihydroxy-3,20-dioxo-9-fluoro-16beta-methyl-17-valeroyloxy-pregna-1,4-dien-21-yl] ester trifluoroacetateHCID 131719968—
SolventDichloromethaneHCID 6344—
ProductN-(N-(N-(N-((1,1-dimethyl)ethoxycarbonyl)-L-alanyl)-L-alanyl)-L-prolyl)-L-valine [9alpha-fluoro-11beta,21-dihydroxy-16beta-methyl-3,20-dioxo-17-valeroyloxy-pregna-1,4-dien-21-yl] esterHCID 13171996763%

Reaction Steps

1.04 g (1.50 mmol) of H-Val-O-BMV x TFA (Example 37), 500 mg (1.40 mmol) of Boc-Ala-Ala-Pro-OH and 168 mg (1.40 mmol) of Nhydroxybenzotriazole are dissolved in this sequence in 50 ml of dichloromethane, and 330 μl (3.00 mmol) of N-methylmorpholine is added. Then, a solution of 289 mg (1.40 mmol) of dicyclohexylcarbodiimide in 2 ml of dichloromethane is added and stirred for 20 hours at room temperature. Then, it is suctioned off from precipitated urea, the filtrate is concentrated by evaporation and filtered again. Chromatography of this amount of raw material (300 g of silica gel, hexane/acetone 1:1) yields 806 mg(63% ) of N-(N-(N-(N-((1,1-dimethyl)ethoxycarbonyl)-L-alanyl) -L-alanyl)-L-prolyl)-L-valine [9α-fluoro-11β,21-dihydroxy-16β-methyl-3,20-dioxo-17-valeroyloxy-pregna-1,4-dien-21-yl ] ester. Crystallization from dichloromethane/diisopropyl ether 542 mg (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616573
Source datasetuspto-grants-1997_04
ORD IDord-397a62ebd1fc4a77a6e0aea178561e5d
Source noteuspto-grants-1997_04