Реакция #66842

Уравнение реакции

tert-butyl 4-chloro-5,6,7,9-tetrahydro-8H-pyrimido[5′,4′:4,5]thieno[2,3-c]azepine-8-carboxylate

tert-Butyl 4-chloro-5,6,7,9-tetrahydro-8H-pyrimido[5′,4′:4,5]thieno[2,3-c]azepine-8-carboxylate

1-(3-fluorobenzyl)-1H-indazol-5-amine

1-(3-Fluorobenzyl)-1H-indazol-5-amine

→

title compound

Выход 63.0%

N-[1-(3-Fluorobenzyl)-1H-indazol-5-yl]-6,7,8,9-tetrahydro-5H-pyrimido[5′,4′:4,5]thieno[2,3-c]-azepin-4-amine

Выход 63.0%

Условия реакции

Обработка

1. 1
   Другоеto yield 213 mg (77% purity, 63% yield), which
2. 2
   Другоеwas used without further purification

Методика

The title compound was synthesized in analogy to Example 12A from tert-butyl 4-chloro-5,6,7,9-tetrahydro-8H-pyrimido[5′,4′:4,5]thieno[2,3-c]azepine-8-carboxylate from Example 80A (200 mg, 0.59 mmol) and 1-(3-fluorobenzyl)-1H-indazol-5-amine from Example 8A (149 mg, 0.62 mmol) to yield 213 mg (77% purity, 63% yield), which was used without further purification.

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