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CAS No. : | 364794-80-9 | MDL No. : | MFCD06797489 |
Formula : | C17H26BNO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | RCGRLLZELIIKDH-UHFFFAOYSA-N |
M.W : | 303.20 | Pubchem ID : | 2795578 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium carbonate;bis-triphenylphosphine-palladium(II) chloride; In water; acetonitrile; at 100℃; for 0.166667 - 0.666667h;Microwave irradiation; | Example 223 2-(lH-indazol-4-yl)-4-morpholino-6-(3-(morpholinomethyl)phenyl)thieno[3,2-d]pyrimidine 299[00823] 2-Chloro-6-iodo-4-morpholinothieno[3,2-£/lpyrimidine 19 (50 mg) was <n="215"/>coupled to 4-[3-(4,4,5,5-tetramethyl-l,332-dioxaborolan-2-yl)]benzylmorpholine, and then reacted with 4-(4,4,5,5-tetramemyl-l,3,2-dioxaborolan-2-yl)-17Wndazole 7 via GeneralProcedure F. The product was purified by reverse phase HPLC to yield 2.6 mg of 299. MS.(Ql) 513.2 (M)+; General Procedure F Suzuki coupling reactions in one pot[00245] 2-CMoro-64odo-4rmorpholmothieno[3,2-£?]pyrimidine 19 (leq), phenylboronic acid or heterocycleboronic acid (R1 -B(OH)2, 1.1 eq) and bis(triphenylphosphine)palladium(II) dichloride (O.leq) in lMNa2CC>3 aqueous solution (3 eq) and acetonitrile (3eq) was heated to 100 0C in a sealed microwave reactor for 10 to 40 min to give 20. Upon completion, 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-lH- indazole 7 (1.3 eq) and bis(triphenylphosphine)palladium(II) dichloride (O.leq) were added in the same pot. The reaction mixture was heated to 150 0C in a sealed microwave reactor for 10 to 15min. The mixture was extracted with ethyl acetate (3 x 5 mL). The combined organic layers were concentrated to yield crude 21. |
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