Реакция #56047

ord-e271d34c4fff4a18b2545544ce4b1a9d

Уравнение реакции

Nc1cc2[nH]ncc2cc1C(=O)O
6-amino-indazole-5-carboxylic acid
Nc1cc2[nH]ncc2cc1C(=O)O
6-Amino-1H-indazole-5-carboxylic acid
Nc1cc2[nH]ncc2cc1C(=O)O
formula 20
Nc1cc2[nH]ncc2cc1C(=O)O
6-Amino-1H-indazole-5-carboxylic acid
NC=O
formamide
O=c1ncnc2cc3[nH][nH]cc3cc12
1H-Pyrazolo[4,5-g]-quinazoline-5-one

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITat a temperature of 180° during another period of 1.5 hours
  2. 2
    ДругоеThe mass obtained
  3. 3
    ФильтрацияThe product was filtered under suction
  4. 4
    Промывкаwashed well with water until the filtrate
  5. 5
    Промывкаwashed with a small amount of ethanol
  6. 6
    ДругоеThe target product (formula 3) was recovered in an amount of 167 mg (36%) in the form of a greyish-brown, finely crystalline material, m.p. 330°

Методика

450 mg (2.5 m-mol) of 6-amino-indazole-5-carboxylic acid (formula 20, prepared according to Example XIII) in 3 ml of formamide were heat-melted and kept at a temperature of 140° during a period of 4.5 hours and then at a temperature of 180° during another period of 1.5 hours. The mass obtained was cooled to room temperature. The product was filtered under suction, washed well with water until the filtrate became clear, and then washed with a small amount of ethanol. The target product (formula 3) was recovered in an amount of 167 mg (36%) in the form of a greyish-brown, finely crystalline material, m.p. 330°. The product was uniform as evidenced by chromatography; pmr (DMSO-d6): δ 7.78, 8.10, 8.44, 8.76 (4 broad s, 4, H3, H4, H7, H9), 11.92, 13.36 (2 with D2O exchangeable broad m, 2, N1H, N6H), (DMSO-d 6 /D2O): δ 7.83, 8.10, 8.45, 8.78 (4 sharp s, 4, H3, H4, H7, H9); ms (70 eV): m/e 186 (100%, M+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04223143uspto-grants-1980_09