Triethylamine → HCID 178436584、化合物

HRID 1524874

反応式

HRID 1524874 の反応式
Br[C:2]1[CH:11]=[CH:10][C:5]([C:6](OC)=[O:7])=[C:4](Cl)[CH:3]=1.[CH3:13][N:14]([P+](ON1N=NC2C=CC=CC1=2)(N(C)C)N(C)C)C.F[P-](F)(F)(F)(F)F.[CH2:40](N(CC)CC)[CH3:41].[NH2:47][C@H:48]([C:56]1[NH:57][CH:58]=[C:59]([C:61]2[CH:69]=[CH:68][C:64]([C:65]([NH2:67])=[O:66])=[CH:63][CH:62]=2)[N:60]=1)[CH2:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1>C1COCC1>[C:65]([C:64]1[CH:63]=[CH:62][C:61]([C:59]2[N:60]=[C:56]([C@@H:48]([NH:47][C:6](=[O:7])[C:5]3[CH:10]=[CH:11][C:2]([C:13]#[N:14])=[CH:3][C:4]=3[CH2:40][CH3:41])[CH2:49][C:50]3[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=3)[NH:57][CH:58]=2)=[CH:69][CH:68]=1)(=[O:66])[NH2:67]

参加物

6

実験手順

The product from Example 143 Part D (90 mg, 0.51 mmol), Bop reagent (265 mg, 0.61 mmol), and triethylamine (0.42 mL, 1.5 mmol) were added together with 5 mL of THF. The mixture was stirred at RT under N2 for 15 minutes and (S)-4-(2-(1-amino-2-phenylethyl)-1H-imidazol-4-yl)benzamide prepared using the methods described in Examples 2 and 28 (365 mg, 0.51 mg) was added. The resulting mixture was heated at 75° C. for 70 minutes. The THF was removed, and the residue was dissolved in EtOAc. It was washed with waster and brine, dried over MgSO4, concentrated, and purified by flash chromatography (silica, EtOAc/hexane) to give 80 mg of the desired product. MS: 464.4 (M+1)+.

後処理

  1. additionwas added
  2. temperatureThe resulting mixture was heated at 75° C. for 70 minutes
  3. customThe THF was removed
  4. dissolutionthe residue was dissolved in EtOAc
  5. washIt was washed with waster and brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated
  8. custompurified by flash chromatography (silica, EtOAc/hexane)

出典と根拠

ORDレコード
ord-1378d686c97e4a38a6072b4f9bb76225
出典データセット
uspto-grants-2015_07
特許番号
US09079860B2

関連ノート

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