Реакция #1726724

ord-9feaee248f394163a1848660df0c3a9b

Уравнение реакции

NC(=O)c1cc(Br)ccc1N
2-amino-5-bromobenzamide
CC(C)(C)OC(=O)N1CCC(=O)CC1
1-Boc-4-piperidone
O=S(=O)(O)O
sulfuric acid
O=C1NC2(CCNCC2)Nc2ccc(Br)cc21
6′-bromospiro-[piperidine-4,2′(1′H)-quinazolin]-4′-(3′H)-one

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe yellow precipitate is collected by filtration
  2. 2
    Промывкаwashed with excess ether
  3. 3
    Другоеdried under vacuum

Методика

A mixture of 33 mg (0.15 mmol) of 2-amino-5-bromobenzamide and 30 mg (0.15 mmol) of 1-Boc-4-piperidone in 400 μL of acetic acid containing 10 μL of sulfuric acid is stirred overnight at room temperature. The reaction mixture is diluted with diethyl ether. The yellow precipitate is collected by filtration, washed with excess ether, and dried under vacuum to give 55 mg (0.15 mmol) of the acetic acid salt of 6′-bromospiro-[piperidine-4,2′(1′H)-quinazolin]-4′-(3′H)-one. MS m/z: 297.0 (M+H)+, 319.0 (M+Na)+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08110570B2uspto-grants-2012_02