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Tert-Butyl nitrite → HCID 11951640、化合物

HRID 1669056
ノート
印刷プレビュー

反応式

HRID 1669056 の反応式
N(OC(C)(C)C)=O.[N+:8]1([O-:22])[C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][C:12]=2[N:11]=[C:10](N)[N:9]=1)[CH2:18][CH2:17][CH2:16]3>CN(C=O)C>[N+:8]1([O-:22])[C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][C:12]=2[N:11]=[CH:10][N:9]=1)[CH2:18][CH2:17][CH2:16]3
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10906Tert-Butyl nitriteHCID 160813107,8-Dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-Oxide

生成物 1

HCID 11951640HCID 11951640、化合物収率 43.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

tert-Butyl nitrite (90%, 2 mL, 14.8 mmol) was added to a stirred solution of amine 19 (1.0 g, 4.95 mmol) in DMF (50 mL) at 60° C. and the solution stirred at 60° C. for 2 h. The solution was cooled to 20° C. and the solvent evaporated. The residue was partitioned between EtOAc (150 mL) and water (150 mL), the organic fraction was washed with water (2×50 mL), washed with brine (50 mL) and dried and the solvent evaporated. The residue was purified by chromatography, eluting with 10% EtOAc/DCM, to give 1-oxide 64 (401 mg, 43%) as a white solid: mp (EtOAc/pet. ether) 130-131° C.; 1H NMR δ 8.91 (s, 1H, H-3), 8.28 (s, 1H, H-9), 7.82 (s, 1H, H-5), 3.11-3.19 (m, 4H, H-6, H-8), 2.24 (p, J=7.5 Hz, 2H, H-7); 13C NMR δ 154.9, 153.0, 150.0, 147.3, 134.6, 123.2, 114.4, 33.2, 32.9, 25.7. Anal. calcd for C10H9N3O: C, 64.2; H, 4.9; N, 22.5. Found: C, 64.1; H, 4.9; N, 22.5%.

後処理

  1. temperatureThe solution was cooled to 20° C.
  2. customthe solvent evaporated
  3. customThe residue was partitioned between EtOAc (150 mL) and water (150 mL)
  4. washthe organic fraction was washed with water (2×50 mL)
  5. washwashed with brine (50 mL)
  6. customdried
  7. customthe solvent evaporated
  8. customThe residue was purified by chromatography
  9. washeluting with 10% EtOAc/DCM

出典と根拠

ORDレコード
ord-1bf6cda46d4f4269b9e43b61ea4dc89b
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989451B2

反応ノート

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