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

Triethylamine → 1-(1H-Imidazol-5-ylmethyl)-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-one

HRID 1171788
ノート
印刷プレビュー

反応式

HRID 1171788 の反応式
Cl.C(O[C:5]([C:7]1[NH:8][CH:9]=[CH:10][C:11]=1[NH2:12])=[O:6])C.[CH:13]([C:15]1[N:16]=[CH:17][NH:18][CH:19]=1)=O.[BH3-]C#N.[Na+].CCN(CC)CC.C([N:39]=[C:40]=[S:41])(=O)C1C=CC=CC=1>CO>[NH:16]1[C:15]([CH2:13][N:12]2[C:11]3[CH:10]=[CH:9][NH:8][C:7]=3[C:5](=[O:6])[NH:39][C:40]2=[S:41])=[CH:19][N:18]=[CH:17]1
参加物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 8471TriethylamineHCID 68284Benzoyl isothiocyanateHCID 764281H-Imidazole-4-carbaldehydeHCID 5003444Sodium cyanoborohydrideHCID 164270913-Amino-2-ethoxycarbonylpyrrole hydrochloride

生成物 1

HCID 116732051-(1H-Imidazol-5-ylmethyl)-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-one
収率 13.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

3-Amino-1H-pyrrole-2-carboxylic acid ethyl ester hydrochloride (0.10 g, 0.52 mmol) was dissolved in methanol (4 mL) and 4-formylimidazole (0.060 g, 0.63 mmol), NaCNBH3 (0.033 g, 0.52 mmol) and Et3N (0.073 g, 0.52 mmol) were added. The resulting mixture was stirred at r.t. overnight. The solvent was removed in vacuo and the residue was dissolved in CH2Cl2 (3 mL) and methanol (1 mL). Benzoyl isothiocyanate (0.078 mL, 0.58 mmol) was added and after stirring at r.t. for 30 minutes the mixture was concentrated in vacuo. The residue was dissolved in ammonia (7N in methanol, 3 mL) and heated at 80° C. for 1 h. The precipitated product was filtered and washed with methanol, followed by diethyl ether. The crude product was purified by preparative HPLC, obtaining 0.017 g (13%) of the title compound as a solid.

後処理

  1. customThe solvent was removed in vacuo
  2. dissolutionthe residue was dissolved in CH2Cl2 (3 mL)
  3. stirringafter stirring at r.t. for 30 minutes the mixture
  4. concentrationwas concentrated in vacuo
  5. dissolutionThe residue was dissolved in ammonia (7N in methanol, 3 mL)
  6. temperatureheated at 80° C. for 1 h
  7. filtrationThe precipitated product was filtered
  8. washwashed with methanol
  9. customThe crude product was purified by preparative HPLC

出典と根拠

ORDレコード
ord-e382b80c542642b49dd8ae5d1ce80f9c
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07829707B2

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