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ChemicalBook CAS DataBase List Tenofovir Impurity 37
161760-03-8

Tenofovir Impurity 37 synthesis

2synthesis methods
31618-90-3 Synthesis
Diethyl (tosyloxy)methylphosphonate

31618-90-3
433 suppliers
$5.00/5g

Tenofovir Impurity 37

161760-03-8
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Yield:161760-03-8 85.8 %

Reaction Conditions:

with water;sodium hydroxide in tetrahydrofuran at 20;

Steps:

4.a a. Synthesis of compounds 4-2

4-1 (2.3g, 7.1360 mmol, 1.0eq) was added to tetrahydrofuran (27.6 mL) andH2O(9.2 mL), then NaOH (2.85 g, 71.3599 mmol, 10.0 eq), RT reaction 2d. The mixture was concentrated under vacuum reduced pressure, and then column chromatography DCM: MeOH = 10: 1-4: 1, to give 1.8g of colorless oily liquid is compound 4-2, yield: 85.8%.

References:

CN114907401,2022,A Location in patent:Paragraph 0075-0078

31618-90-3 Synthesis
Diethyl (tosyloxy)methylphosphonate

31618-90-3
433 suppliers
$5.00/5g

161760-09-4 Synthesis
Tenofovir Impurity 38

161760-09-4
27 suppliers
inquiry

Tenofovir Impurity 37

161760-03-8
22 suppliers
inquiry

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