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Formic Acid → HCID 178429600、化合物

HRID 906101
ノート
印刷プレビュー

反応式

HRID 906101 の反応式
[NH2:1][C:2]1[C:3]([CH3:13])=[C:4]([CH:9]=[CH:10][C:11]=1[NH2:12])[C:5]([O:7]C)=[O:6].[CH:14](O)=O>>[CH3:13][C:3]1[C:2]2[NH:1][CH:14]=[N:12][C:11]=2[CH:10]=[CH:9][C:4]=1[C:5]([OH:7])=[O:6]
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

3

反応物 2

HCID 284Formic AcidHCID 67403564Methyl 3,4-diamino-2-methylbenzoate

生成物 1

HCID 178429600HCID 178429600、化合物

反応条件

温度
70 °C

実験手順

Methyl 3,4-diamino-2-methylbenzoate (synthesized in reagent preparation 22) (0.18 g, 1.0 mmol) was taken up in formic acid (8.0 mL) and refluxed for 4 hours. The solution was then concentrated in vacuo. The material was taken up in methanol (2.5 mL) and tetrahydrofuran (5.0 mL) and treated with 2M aqueous lithium hydroxide (2.5 mL) and heated to 70° C. for 12 hours. This solution was made acidic using concentrated aqueous hydrochloric acid, then extracted with 10% methanol in ethyl acetate (2×50 mL). The combined organic layers were dried (magnesium sulfate), filtered and concentrated to give 0.055 g of 7-methyl-1H-benzimidazole-6-carboxylic acid. 1H NMR (400 MHz, d6-DMSO): 9.34 (s, 1H), 7.94 (d, 1H), 7.64 (d, 1H), 2.85 (s, 3H). MS (EI) for C9H8N2O2: 177 (MH+).

後処理

  1. temperaturerefluxed for 4 hours
  2. concentrationThe solution was then concentrated in vacuo
  3. additiontetrahydrofuran (5.0 mL) and treated with 2M aqueous lithium hydroxide (2.5 mL)
  4. extractionextracted with 10% methanol in ethyl acetate (2×50 mL)
  5. dry with materialThe combined organic layers were dried (magnesium sulfate)
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-f96840c3bc864e74ab4533a3995347ee
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012956B2

反応ノート

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