ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → HCID 46931261、化合物

HRID 1097197
ノート
印刷プレビュー

反応式

HRID 1097197 の反応式
[OH-].[NH4+:2].[CH3:3][N:4]([N:6]=[N:7][C:8]1[CH:9]=[C:10]([C:14]([O:16]C)=O)[Se:11][C:12]=1[CH3:13])[CH3:5].O>C1COCC1>[CH3:3][N:4]([N:6]=[N:7][C:8]1[CH:9]=[C:10]([C:14]([NH2:2])=[O:16])[Se:11][C:12]=1[CH3:13])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 14923Ammonium HydroxideHCID 59547219HCID 59547219、化合物

生成物 1

HCID 46931261HCID 46931261、化合物収率 42%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To an ice cold (0-5° C.) solution of ammonium hydroxide (40 mL) was added a solution of methyl 4-[(dimethylamino)diazenyl]-5-methylselenophene-2-carboxylate (550 mg) in THF (10 mL) for 5 min and stirred at rt for 40 h. The solution was poured into ice cooled water and extracted with chloroform (3×100 mL). The combined organic layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform-methanol (96:4) as eluents to give the product as off-white solid (220 mg, 42%), mp 170-172° C. IR (neat) νmax 3385, 3188, 2914, 1644, 1604, 1326, 1120, 1066 cm−1; 1H NMR (400 MHz, CDCl3): δ 7.87 (1H, s, H-3), 5.67 (2H, br s, —CONH2), 3.28 (6H, br s, N(CH3)2), 2.63 (3H, s, Ar—CH3); LC-MS (positive ion mode): m/z 261, 259 (M+H)+.

後処理

  1. additionThe solution was poured into ice
  2. extractionextracted with chloroform (3×100 mL)
  3. washThe combined organic layer was washed with water, brine
  4. dry with materialdried over sodium sulfate
  5. filtrationThe solution was filtered
  6. customevaporated the solvent
  7. customThe residue was chromatographed over silica gel column

出典と根拠

ORDレコード
ord-3ebf81c2000f459b8b91cc5244e85e96
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08143237B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート