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Water → 1h-Indazole-1-carboxylic acid,3-[(4-ethylphenyl)methyl]-,1,1-dimethylethyl ester

HRID 1625861
ノート
印刷プレビュー

反応式

HRID 1625861 の反応式
O1C=CC=C1P(C1OC=CC=1)C1OC=CC=1.[C:17]([O:21][C:22]([N:24]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26](I)=[N:25]1)=[O:23])([CH3:20])([CH3:19])[CH3:18].[Br-].[CH2:35]([C:37]1[CH:44]=[CH:43][C:40]([CH2:41][Zn+])=[CH:39][CH:38]=1)[CH3:36].O>O1CCCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[C:17]([O:21][C:22]([N:24]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26]([CH2:41][C:40]2[CH:43]=[CH:44][C:37]([CH2:35][CH3:36])=[CH:38][CH:39]=2)=[N:25]1)=[O:23])([CH3:20])([CH3:19])[CH3:18]
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 4

HCID 962WaterHCID 521585Tris(furan-2-yl)phosphaneHCID 11473390tert-butyl 3-iodo-1H-indazole-1-carboxylateHCID 178436323HCID 178436323、化合物

生成物 1

HCID 666081711h-Indazole-1-carboxylic acid,3-[(4-ethylphenyl)methyl]-,1,1-dimethylethyl ester

試薬・触媒・溶媒 2

HCID 9811564
Bis(dibenzylideneacetone)palladium
触媒
HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of tris(dibenzylideneacetone)dipalladium (0) (167 mg) and tri(2-furyl)phosphine (135 mg) in tetrahydrofuran (20 ml) was stirred at room temperature for 5 minutes under argon atmosphere. Thereto were added 1-t-butoxycarbonyl-3-iodo-1H-indazole (2.0 g) and the above 4-ethylbenzylzinc bromide (N,N-dimethylformamide solution) at 0° C., and the mixture was stirred at room temperature for 5 hours. The reaction mixture was poured into water, and the mixture was extracted with diethyl ether. The extract was washed with water and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0-92:8) to give 1-t-butoxycarbonyl-3-(4-ethylphenylmethyl)-1H-indazole (1.37 g) as colorless oil. APCI-Mass m/Z 337 (M+H).

後処理

  1. extractionthe mixture was extracted with diethyl ether
  2. washThe extract was washed with water
  3. dry with materialdried over magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0-92:8)

出典と根拠

ORDレコード
ord-85d24b43aba44a44bcf5dace3a2bde71
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785403B2

反応ノート

読み込み中…

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