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ChemicalBook CAS DataBase List tert-Butyl N-(1,3-benzothiazol-2-ylMethyl)carbaMate

tert-Butyl N-(1,3-benzothiazol-2-ylMethyl)carbaMate synthesis

3synthesis methods
-

Yield:864738-25-0 78%

Reaction Conditions:

with iodine at 20; for 0.333333 h;

Steps:

Benzothiazoles 3a-3f and 4a-4f from N-protected amino acids (general procedure).

General procedure: The reaction between protected amino acid (500 mg, 2.7 mmol) and 2-aminothiophenol (0.67 mL, 5.3 mmol) in the presence of iodine (223 mg, 1.8 mmol) as a catalyst was carried out following the procedure described in [14]. The reaction was complete (TLC monitoring) in 20 min. The product was washed with aqueous Na2S2O3 to removeunreacted iodine and purified by recrystallization from a 70 : 30 ethanol-water mixture.

References:

Arfan, M.;Fatima, T.;Mannan, A.;Tahira, A. [Russian Journal of Organic Chemistry,2020,vol. 56,# 2,p. 292 - 297]

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