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

Acetic Acid → 4-[2-(3,5,5-Trimethyl-2-oxoimidazolidin-1-yl)-1,3-thiazol-4-yl]benzonitrile

HRID 1436425
ノート
印刷プレビュー

反応式

HRID 1436425 の反応式
[CH3:1][C:2]([NH:6][C:7]1[S:8][CH:9]=[C:10]([C:12]2[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][CH:13]=2)[N:11]=1)([CH3:5])[CH:3]=O.[C:20]([OH:23])(=O)C.CN.[C:26]([BH3-])#[N:27].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(N(CC)CC)C.ClC(Cl)(OC(=O)OC(Cl)(Cl)Cl)Cl.C([O-])(O)=O.[Na+]>CO.C(OCC)(=O)C.O1CCCC1.C(Cl)Cl>[CH3:26][N:27]1[CH2:3][C:2]([CH3:5])([CH3:1])[N:6]([C:7]2[S:8][CH:9]=[C:10]([C:12]3[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][CH:13]=3)[N:11]=2)[C:20]1=[O:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

13

反応物 8

HCID 176Acetic AcidHCID 6329MethylamineHCID 8471TriethylamineHCID 94429TriphosgeneHCID 516892Sodium BicarbonateHCID 5003444Sodium cyanoborohydrideHCID 5049666Sodium triacetoxyborohydride
HCID 86618609
4-{2-[(1,1-Dimethyl-2-oxoethyl)amino]-1,3-thiazol-4-yl}benzonitrile

生成物 1

HCID 247832464-[2-(3,5,5-Trimethyl-2-oxoimidazolidin-1-yl)-1,3-thiazol-4-yl]benzonitrile収率 28.7%

試薬・触媒・溶媒 4

HCID 887Methanol溶媒2 回HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

実験手順

4-{2-[(1,1-dimethyl-2-oxoethyl)amino]-1,3-thiazol-4-yl}benzonitrile (318 mg, 1.17 mmol), prepared in the previous step, was dissolved in 12 mL of methanol and 1 g of molecular sieves was added. Acetic acid (0.13 mL, 2.3 mmol) and a 2M solution of methylamine in methanol (1.76 mL, 3.52 mmol) were added followed by sodium cyanoborohydride (0.44 g, 7.0 mmol) and the mixture was stirred for 16 h. Sodium triacetoxyborohydride (1.5 g, 7.0 mmol) was added and the mixture was stirred for 72 h. The mixture was diluted with ethyl acetate and washed with H2O, NaHCO3, brine, dried over anhydrous MgSO4, filtered and concentrated to give 380 mg of crude product. This material was dissolved in 15 mL tetrahydrofuran and triethylamine (1.0 mL, 7.3 mmol) was added followed by triphosgene (0.59 g, 2.0 mmol). The mixture was stirred for 2 h, poured into saturated NaHCO3, diluted with methylene chloride and washed with H2O, 1N HCl, brine, dried over anhydrous MgSO4, filtered and concentrated. Flash chromatography (20% ethyl acetate/hexane) afforded the title compound (0.105 g, 25%) as a white solid. HRMS: calcd for C16H16N4OS+H+, 313.11176; found (ESI, [M+H]+), 313.1104; Analytical HPLC: purity 100% at 210-370 nm, 9.7 min; 100% at 252 nm, 9.7 min; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammon. Form. Buff. pH=3.5/ACN+MeOH) for 10 min, hold 4 min.

後処理

  1. addition1 g of molecular sieves was added
  2. stirringthe mixture was stirred for 72 h
  3. washwashed with H2O, NaHCO3, brine
  4. dry with materialdried over anhydrous MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto give 380 mg of crude product
  8. stirringThe mixture was stirred for 2 h
  9. washwashed with H2O, 1N HCl, brine
  10. dry with materialdried over anhydrous MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated

出典と根拠

ORDレコード
ord-13c93d076376402fb5113099b420f103
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07618990B2

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