Acetic Acid → 5-Amino-1-(3-chloro-4-[4-chlorobenzoyl]-5-methylbenzyl)-1,2,3-triazole-4-carboxamide

HRID 280676노트

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HRID 280676 반응식
[Na].[C:2]([CH2:4][C:5]([NH2:7])=[O:6])#[N:3].[Cl:8][C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([CH3:28])[C:18]=1[C:19](=[O:27])[C:20]1[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=1)[CH2:12][N:13]=[N+:14]=[N-:15].C(O)(=O)C>C(O)C>[NH2:3][C:2]1[N:13]([CH2:12][C:11]2[CH:16]=[C:17]([CH3:28])[C:18]([C:19](=[O:27])[C:20]3[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=3)=[C:9]([Cl:8])[CH:10]=2)[N:14]=[N:15][C:4]=1[C:5]([NH2:7])=[O:6]

참가 물질

6

실험 절차

A stirred, 60° C. solution of sodium (88.7 mg, 3.84 mmol) in absolute ethanol (9.6 ml) was treated with 2-cyanoacetamide (323 mg, 3.84 mmol), kept 5 min., and treated with 3-chloro-4-(4-chlorobenzoyl)-5-methylbenzyl azide (1.03 g, 3.20 mmol). The mixture was refluxed 1 hour, cooled to ambient temperature, acidified with glacial acetic acid (487 μl, 511 mg, 7.68 mmol), and evaporated to dryness at 30° C. under vacuum. The residue was chromatographed on a column of silica gel (150 g) eluted in 17 ml fractions with 19:1 (v/v) dichloromethane-methanol. Fractions 22-38 were combined and evaporated to dryness. The residual glass was kept 18 hours at ambient temperature with diethyl ether (25 ml), filtered, washed with diethyl ether, and dried to provide 870 mg (67%) crystalline 5-amino-1-(3-chloro-4-[4-chlorobenzoyl]-5-methylbenzyl)-1,2,3-triazole-4 -carboxamide, m.p. 205°-206° C.

후처리

  1. temperatureThe mixture was refluxed 1 hour
  2. customevaporated to dryness at 30° C. under vacuum
  3. customThe residue was chromatographed on a column of silica gel (150 g)
  4. washeluted in 17 ml fractions with 19:1 (v/v) dichloromethane-methanol
  5. customevaporated to dryness
  6. waitThe residual glass was kept 18 hours at ambient temperature with diethyl ether (25 ml)
  7. filtrationfiltered
  8. washwashed with diethyl ether
  9. customdried

출처 및 근거

ORD 기록
ord-9b62d756e4a44b1ab9e811dfda3503a7
출처 데이터셋
uspto-grants-1986_05
특허 번호
US04590201

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