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Tetrahydrofuran → 1-Methylpyridin-1-ium 4-methylbenzenesulfonate

HRID 962920
Notes
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Reaction equation

HRID 962920 reaction equation
CC1[C@@H](OC([C@H](O)[C@@H:24]([NH:31][C:32]([C:34]2[CH:35]=[CH:36][CH:37]=CC=2)=O)C2C=CC=CC=2)=O)C[C@]2(O)C(C)(C)C=1[C@@H](OC(C)=O)C([C@@]1(C)[C@H]([C@@H]2OC(C2C=CC=CC=2)=O)[C@]2(OC(C)=O)CO[C@@H]2C[C@@H]1O)=O.C(N(CC)CC)C.[S:70]([C:74]1[CH:80]=[CH:79][C:77]([CH3:78])=[CH:76][CH:75]=1)([O-:73])(=[O:72])=[O:71].FC1C=CC=C[N+]=1C.O1CCCC1>OP(O)=O.O[Mo](O)(=O)=O.O>[S:70]([C:74]1[CH:80]=[CH:79][C:77]([CH3:78])=[CH:76][CH:75]=1)([O-:73])(=[O:72])=[O:71].[CH3:24][N+:31]1[CH:32]=[CH:34][CH:35]=[CH:36][CH:37]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 36314Paclitaxel2×HCID 1716312-Fluoro-1-methylpyridinium p-toluenesulfonate

Product 1

HCID 115218291-Methylpyridin-1-ium 4-methylbenzenesulfonate

Reagents, catalysts & solvents 2

HCID 21863154
Dihydroxy(dioxo)molybdenum;phosphonic acid
Catalyst
HCID 962WaterSolvent

Procedure

Taxol-2'-MPT (methylpyridinium tosylate) was synthesized according to the method of T. Mukaiyama, Angewandte Chemie 1979, 18(18), 707-808. Taxol (10 mg, 0.012 mM), from NaPro Biochemicals, Boulder Colo., USA, was dried by azeotropic distillation with toluene (2×1.0 mL) and then dissolved in methylene chloride (0.4 mL) and treated sequentially under an atmosphere of dry argon, with freshly distilled triethylamine (5 microL, 0.04 mM, 3 equivalents) and 2-fluoro-1-methylpyridinium tosylate (5 mg, 0.018 mM, 1.5 equivalents) Aldrich Chemicals, and allowed to stir at ambient temperature for 30 minutes. The clear colorless solution rapidly turned to a clear pale yellow. The course of the reaction was monitored through thin layer chromatography (TLC) (E. Merck RP-18 silica, 65 tetrahydrofuran:35 water, UV/phosphomolybdic acid) and after thirty minutes of stirring at ambient temperature, judged complete as no taxol remained and only one compound was apparent by TLC (Rf 0.8). Purification via reverse phase high pressure liquid chromatography (HPLC) (C18 column, 1 mM NH4OAc pH 6.5 buffer/methanol gradient, 1.5 mL/min. UV) to give, after removal of solvent in vaccuo, pure taxol-2'-MPT (2) (12 mg, 93% yield) as a white amorphous solid. All spectroscopic data (1H NMR and HRMS) were in accord with the structure assigned to taxol-2'-MPT. 1H NMR (CDCl3, 125 MHz) δ: 1.055 (s, 3H, C17-H), 1.083 (s, 3H, C19-H), 1.724 (s, 3H, C19-H), 1.858 (m, 1H, C6-βH), 1.913 (s, 3H, CH3 -Ph), 2.193 (s, 3H, C10-OC(O)CH3), 2.514 (m, 1H, C6-aH), 3.663 (d, 1H, J=7.0 Hz, C3-H), 4.110 (d, 1H, J=8.5, C20-aH, A of AB), 4.133 (s, 3H, N--CH3), 4.230 (d, 1H, J=8.5, C20-aH, B of AB), 4.315 (dd, 1H, J=8.7, 10.7, C7-H), 4.901 (dd, 1H, J=1.0, 7.7, C5-H), 5.501 (d, 1H, C2-H, J=7.0), 5.702 (bt, 1H, C2'-H, J=8.0), 5.951 (dd, 1H, C13-H, J=1.0, 8.0), 6.120 (bd, 1H, C3'-H, J=10.0), 6.181 (s, 1H, C10-H) 7.702 (t, 1H, N--H, J=7.5), 7.33-7.45 (m, 8H, Ar--H), 7.56-7.62 (m, 4H, Ar--H), 7.56-7.62 (m, 4H, Ar--H), 7.68-7.75 (m, 4H, Ar--H), 8.00-8.05 (m, 1H Ar--H), 8.23-8.28 (m, 1H, Pyr-H), 8.41 (m, 1H, Pyr-H). IR (neat, KCl plate) cm-1 : 3640-3120 (bm), 3030-2870 (bm), 2320 (m), 1720 (s), 1630 (m), 1560 (m), 1500 (m), 1360 (s), 1160 (m), 1070 (m), 700 (m). UV/Vis (CHCl3) nm: 254, 280. FAB HRMS: calc for C53H57 O14N2 : 945.3810; found: 945.3810.

Workup

  1. dry with material, USA, was dried by azeotropic distillation with toluene (2×1.0 mL)
  2. dissolutiondissolved in methylene chloride (0.4 mL)
  3. stirringof stirring at ambient temperature
  4. customPurification via reverse phase high pressure liquid chromatography (HPLC) (C18 column, 1 mM NH4OAc pH 6.5 buffer/methanol gradient, 1.5 mL/min. UV)
  5. customto give

Sources & evidence

ORD record
ord-94f14f95c1c94c8282cf93fb6b9c0509
Source dataset
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05760240

Reaction notes

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