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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991024Generated: October 26, 2026

Ninhydrin → Tacrolimus

https://huagongshe.com/reaction/1991024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNinhydrinHCID 10236—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 72524391HCID 72524391—
Reactantacetic anhydride DMFHCID 86761394—
SolventBenzeneHCID 241—
Solventdichloromethane N-methyl-2-pyrrolidoneHCID 19383075—
ProductTacrolimusHCID 445643—

Reaction Steps

The syrup obtained in Example 1 was centrifuged with benzene and concentrated under reduced pressure, and dissolved in a mixed solvent of methylene chloride/N-methyl-2-pyrrolidone (4/1) (0.3 ml), and WSC (1.44 mg, 7.5 μmol) and 1-hydroxybenzotriazole (1.01 mg, 7.5 μmol) were added. This solution was added to 10 μl of TOYO-Pearl resin (TSKgel AF-amino; 0.01 mmol amine is present in 100 μl) and shaken at room temperature overnight. After completion of the reaction, the resin was thoroughly washed with a mixed solvent of methylene chloride/N-methyl-2-pyrrolidone (4/1), and DMF, and the percent condensation yield was determined by the ninhydrin test (about 29%). A mixed solution of acetic anhydride/DMF (1/4) (0.3 ml) was added to the resin obtained, and this was followed by shaking at room temperature for 30 minutes. After completion of the reaction, the resin was thoroughly washed with methylene chloride, dimethylformamide (DMF) and 20% aqueous ethanol, and this resin was used as the affinity resin in the subsequent experiments.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645614B2
Source datasetuspto-grants-2010_01
ORD IDord-667291f776064bb6b6d0d90a4de81add
Source noteuspto-grants-2010_01