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

Guaiacol → HCID 22054602、化合物

HRID 1006142
ノート
印刷プレビュー

反応式

HRID 1006142 の反応式
CC(OC(/N=N/C(OC(C)C)=O)=O)C.Cl[C:16]1[C:25]2[C:20](=[CH:21][C:22]([CH2:26][OH:27])=[CH:23][CH:24]=2)[N:19]=[C:18]([CH3:28])[CH:17]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1O.[NH:57]1[CH2:61][CH2:60][CH2:59][CH2:58]1.[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64]>ClCCl.C(O)C>[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64].[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1[O:27][CH2:26][C:22]1[CH:21]=[C:20]2[C:25]([C:16]([N:57]3[CH2:61][CH2:60][CH2:59][CH2:58]3)=[CH:17][C:18]([CH3:28])=[N:19]2)=[CH:24][CH:23]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 460GuaiacolHCID 971Oxalic AcidHCID 11776TriphenylphosphineHCID 31268PyrrolidineHCID 5363146Diisopropyl azodicarboxylateHCID 11264243HCID 11264243、化合物

生成物 1

HCID 22054602HCID 22054602、化合物
収率 43%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 6344Dichloromethane溶媒

実験手順

Diisopropylazodicarboxylate (97 mg, 0.48 mmol) was added dropwise at r.t. to a solution of (4-chloro-2-methyl-quinolin-7-yl)-methanol (example 2c, 100 mg, 0.48 mmol), triphenylphosphine (126 mg, 0.48 mmol), 2-methoxyphenol (60 mg, 0.48 mmol) in dichloromethane (2.5 mL). After shaking 24 h at r.t., the solvent was evaporated, and the residue was taken up in pyrrolidine (1.37 g, 19.2 mmol) and shaken for 23 h at 80° C. After cooling the reaction mixture was partitioned between sat. aq. ammonium chloride solution and dichloromethane, the organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which was dissolved in ethanol and treated with 20% ethanolic oxalic acid solution. The precipitate was collected by filtration and dried to afford the title compound (90 mg, 43%). Off-white solid, ISP-MS: m/e=349.4 ([M+H—C2H2O4]+).

後処理

  1. customthe solvent was evaporated
  2. stirringshaken for 23 h at 80° C
  3. temperatureAfter cooling the reaction mixture
  4. customwas partitioned between sat. aq. ammonium chloride solution and dichloromethane
  5. washthe organic layer was washed with brine
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. customChromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which
  9. filtrationThe precipitate was collected by filtration
  10. customdried

出典と根拠

ORDレコード
ord-3460d1419998418fbea719f32b1273b2
出典データセット
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06787558B2

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