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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991023Generated: October 26, 2026

Tacrolimus-13C,D2 → HCID 72524391, compound

https://huagongshe.com/reaction/1991023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTacrolimus-13C,D2HCID 5372—
ReactantHydrofluoric AcidHCID 14917—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 23084396HCID 23084396—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 72524391HCID 72524391—

Reaction Steps

17-allyl-1,14-di-hydroxy-12-[2-(4-hydroxy-3-methoxy-cyclohexyl)-1-methyl-vinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-aza-tricyclo[22.3.1.04,9] octacos-18-ene-2,3,10,16-tetraone (FK-506, 1, 3.3 mg, 4.10 μmol) was twice boiled together with benzene, and dissolved in dichloromethane (39 μl), and 16.2 μl (4.09 μmol) of a solution of O-mono(tert-butyl-diphenyl-silanyl)octanedioic acid in dichloromethane (100 mg/ml) was added. After this was dissolved by the addition of 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (WSC/HCl, 0.94 mg, 4.90 μmol) and 23 μl (1.88 μmol) of a solution of 4-dimethylaminopyridine in dichloromethane (10 mg/ml) at room temperature, the solution was allowed to stand for 1.5 hours. This solution was extracted by the addition of dichloromethane (150 μl) and saturated aqueous sodium carbonate (150 μl). The organic phase collected was concentrated by blowing a nitrogen stream. After the syrup obtained was dissolved by the addition of acetonitrile (28 μl), 46-48% aqueous hydrogen fluoride (6.5 μl) was added at room temperature, and the solution was allowed to stand for 1.5 hours. This solution was extracted by the addition of ethyl acetate (100 μl) and saturated aqueous sodium carbonate (100 μl), and the organic phase was concentrated by blowing a nitrogen stream, to yield a syrup of mixture A. The mixture A was used as is without purification and the like in the next step. The mixture A was used while no structural information was available about whether or not the mixture A contains a compound having the spacer introduced thereto only at a position where the binding to FKBP12 is not affected, for example, 17-allyl-1,14-di-hydroxy-12-{2-[4-(7-carboxy-heptanoyl-oxy)-3-methoxy-cyclohexyl]-1-methyl-vinyl}-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-aza-tricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetraone shown in Reference Production Example 2, or contains FK506 having the spacer introduced therein at a position where there is a contribution to the binding to FKBP12, or contains FK506 having a plurality of spacers introduced thereto, and the like.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645614B2
Source datasetuspto-grants-2010_01
ORD IDord-0a990ec682894841a59cc096cd217636
Source noteuspto-grants-2010_01