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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879267Generated: October 31, 2026

Lithium Hydroxide → (9R,11S,14S,20E)-14-cyclohexyl-13-oxo-8-oxa-12,15-diazatetracyclo[20.3.1.12,6.19,12]octacosa-1(26),2(28),3,5,20,22,24-heptaene-11-carboxylic acid

https://huagongshe.com/reaction/1879267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantmethyl (9R, 11S, 14S,20E)-14-cyclohexyl-13-oxo-8-oxa-12,15-diazatetracyclo[20.3.1.12,6.19,12]octacosa-1(26),2(28),3,5,20,22,24-heptaene-11-carboxylateHCID 58005169—
SolventEthanol tetrahydrofuran waterHCID 18504229—
Product(9R,11S,14S,20E)-14-cyclohexyl-13-oxo-8-oxa-12,15-diazatetracyclo[20.3.1.12,6.19,12]octacosa-1(26),2(28),3,5,20,22,24-heptaene-11-carboxylic acidHCID 58005172—

Reaction Conditions

Temperature40 °C

Reaction Steps

LiOH (3.0 eq.) was added to a 0.04M solution of methyl (9R,11S,14S,20E)-14-cyclohexyl-13-oxo-8-oxa-12,15-diazatetracyclo[20.3.1.12,6.19,12]octacosa-1(26),2(28),3,5,20,22,24-heptaene-11-carboxylate 110 in a mixture of THF:EtOH:H2O (2:1:1) and the reaction mixture was stirred at 40° C. for 2 h. The solvents were removed under reduced pressure, the residue was suspended in EtOAc/H2O, aqueous (1N) HCl was added to acidic pH and the phases separated. The collected organic layers were dried (Na2SO4) and evaporated under reduced pressure to afford a residue which was used without further purification. MS (ES+) m/z 517 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314062B2
Source datasetuspto-grants-2012_11
ORD IDord-0a3401424a61463ebcf42a1c5d6ced61
Source noteuspto-grants-2012_11