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Ammonium Bicarbonate → HCID 178513575、化合物

HRID 2247152
ノート
印刷プレビュー

反応式

HRID 2247152 の反応式
[C:1]1([C:7]2([C:12]3[CH:17]=[CH:16][C:15]([C:18]4[NH:22][C:21]5[CH:23]=[CH:24][C:25]([C:27]([NH2:29])=[O:28])=[CH:26][C:20]=5[N:19]=4)=[CH:14][CH:13]=3)[O:11][CH2:10][CH2:9][O:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:30]C1C=CC(C2(C3C=CC(C4NC5C=CC(C(O)=O)=CC=5N=4)=CC=3)OCCO2)=CC=1.C(N1C=CN=C1)(N1C=CN=C1)=O.C(=O)(O)[O-].[NH4+].[NH4+].[Cl-]>CN(C=O)C>[Cl:30][C:4]1[CH:3]=[CH:2][C:1]([C:7]2([C:12]3[CH:17]=[CH:16][C:15]([C:18]4[NH:22][C:21]5[CH:23]=[CH:24][C:25]([C:27]([NH2:29])=[O:28])=[CH:26][C:20]=5[N:19]=4)=[CH:14][CH:13]=3)[O:8][CH2:9][CH2:10][O:11]2)=[CH:6][CH:5]=1
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

7

反応物 5

HCID 14013Ammonium BicarbonateHCID 25517Ammonium ChlorideHCID 682631,1'-CarbonyldiimidazoleHCID 178513574HCID 178513574、化合物HCID 178524154HCID 178524154、化合物

生成物 1

HCID 178513575HCID 178513575、化合物収率 76%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

2-[4-(2-Phenyl-[1,3]dioxolan-2-yl)-phenyl]-1H-benzoimidazole-5-carboxylic acid amide. To a solution of 2-{4-[2-(4-chloro-phenyl)-[1,3]dioxolan-2-yl]-phenyl}-1H-benzoimidazole-5-carboxylic acid (135 mg, 0.32 mmol) in anhydrous DMF was added carbonyldiimidazole (118 mg, 0.73 mmol). The reaction mixture was stirred under N2 for 30 min and then cooled to 0° C., and ammonium bicarbonate (140 mg, 1.4 mmol) was added. The resulting mixture was allowed to warm to RT and was stirred for 16 h. The mixture was added dropwise to saturated aqueous NH4Cl. The resulting precipitate was collected by filtration and washed with H2O (100 mL) then hexanes (100 mL). The product was dried under vacuum overnight to give the title compound (1.02 mg, 76%). TLC (silica, 1% methanol saturated with ammonia/9% methanol/CH2Cl2): Rf=0.33. HPLC (Method A): Rt=7.42. MS (ESI+): mass calculated for C23H18ClN3O3, 419.1; m/z found, 420.1 [M+H]+. 1H NMR (400 MHz, CD3OD): δ 8.09 (s, 1H), 8.00 (d, J=8.4 Hz, 2H), 7.75-7.72 (dd, J=8.5, 1.5 Hz, 1H), 7.59 (d, J=8.4 Hz, 2H), 7.56 (br d, J=8.7 Hz, 1H), 7.43 (d, J=8.5 Hz, 2H), 7.27 (d, J=8.6 Hz, 2H), 3.99 (s, 4H).

後処理

  1. temperatureto warm to RT
  2. stirringwas stirred for 16 h
  3. filtrationThe resulting precipitate was collected by filtration
  4. washwashed with H2O (100 mL)
  5. customThe product was dried under vacuum overnight

出典と根拠

ORDレコード
ord-c51e1f1db9984c1c865b35aaf9150f00
出典データセット
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07687639B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート