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ChemicalBook CAS DataBase List Mc-Val-Cit-PABC-PNP
159857-81-5

Mc-Val-Cit-PABC-PNP synthesis

14synthesis methods
159857-80-4 Synthesis
MC-Val-Cit-PAB

159857-80-4
182 suppliers
$27.00/1mg

5070-13-3 Synthesis
BIS(4-NITROPHENYL) CARBONATE

5070-13-3
248 suppliers
$5.00/5g

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Yield:159857-81-5 95%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in N,N-dimethyl-formamide at 25;

Steps:

6 Example 6. Synthesis of mc-Val-Cit-PABC-PNP
mc-Val-Cit-PABOH (1 eq.) was mixed with bis(4-nitrophenyl) carbonate (1.87 eq.) in N,N-dimethylformamide (8 vol.) at 20°C. N,N-diisopropyl ethyl amine (1.75 eq.) was added at 25°C. The reaction mixture was stirred at 25°C for 2-6 hours until reaction was complete. Product was precipitated out of the reaction mixture by adding anhydrous ethyl acetate (12.5 vol.) at 25°C and tert-Butyl methyl ether (12.5 vol.). The resulting slurry was stirred, then cooled to 0°C and stirred for 10-30 minutes. The solids were isolated by filtration, washed and dried under vacuum before being re-slurried in ethyl acetate (12.5 vol.) at 20°C, filtered and dried once more (95% yield). MS: m/e 738 (MH)+, 760 (M+Na)+.

References:

SEATTLE GENETICS, INC.;BLANCHARD, Sophie;COATS, James WO2019/108797, 2019, A1 Location in patent:Paragraph 0117

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