Benzyl Alcohol → HCID 67203361、化合物

HRID 85104ノート

反応式

HRID 85104 の反応式
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:4]=[C:5]([C:9]2[NH:13][C:12]3[CH:14]=[CH:15][CH:16]=[C:17](C(O)=O)[C:11]=3[N:10]=2)[CH:6]=[CH:7][CH:8]=1.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:30])C=CC=CC=1.CC[N:42]([CH2:45]C)CC.[CH2:47]([OH:54])[C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1>C1(C)C=CC=CC=1>[F:21][C:2]([F:22])([F:1])[C:3]1[CH:4]=[C:5]([C:9]2[NH:13][C:12]3[CH:14]=[CH:15][CH:16]=[C:17]([NH:42][C:45](=[O:30])[O:54][CH2:47][C:48]4[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=4)[C:11]=3[N:10]=2)[CH:6]=[CH:7][CH:8]=1

参加物

6

実験手順

A solution of 2-(3-(trifluoromethyl)phenyl)-1H-benzo[d]imidazole-4-carboxylic acid (11; 1.53 g, 5.0 mmol), diphenylphosphoryl azide (DPPA, 1.39 g, 5.0 mmol) and Et3N (0.75 g, 7.4 mmol) in toluene (15 mL) was stirred at room temperature for 2 h and then stirred under reflux for 2 h. Benzyl alcohol (0.54 g, 5.0 mmol) was added and the resulting reaction mixture was stirred under reflux for another 12 h. After cooling to room temperature, the mixture was washed successively with aqueous citric acid (10% w/w), saturated NaHCO3 and brine. The organic layer was (Na2SO4), and concentrated under reduced pressure. The resulting residue was purified by chromatography (petroleum ether:ethyl acetate=10:1) to give benzyl 2-(3-(trifluoromethyl)phenyl)-1H-benzo[d]imidazol-4-ylcarbamate 12 (1.45 g, 70%) as a solid. MS (ESI) calcd for C22H16F3N3O2: 411.12; found: 412 [M+H].

後処理

  1. temperatureunder reflux for 2 h
  2. customthe resulting reaction mixture
  3. stirringwas stirred
  4. temperatureunder reflux for another 12 h
  5. washthe mixture was washed successively with aqueous citric acid (10% w/w), saturated NaHCO3 and brine
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by chromatography (petroleum ether:ethyl acetate=10:1)

出典と根拠

ORDレコード
ord-a1b20383c4ee4aca8b7d133a45c2a7f2
出典データセット
uspto-grants-2014_09
特許番号
US08846947B2

反応ノート

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