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Water → Ethyl-4-ethoxy-1-(pent-4-ynyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

HRID 1252700
ノート
印刷プレビュー

反応式

HRID 1252700 の反応式
[CH2:1]([O:3][C:4]1[C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:8][N:7]=[C:6]2[NH:15][N:16]=[CH:17][C:5]=12)[CH3:2].I[CH2:19][CH2:20][CH2:21][C:22]#[CH:23].C(=O)([O-])[O-].[K+].[K+].O>CN(C=O)C>[CH2:13]([O:12][C:10]([C:9]1[C:4]([O:3][CH2:1][CH3:2])=[C:5]2[CH:17]=[N:16][N:15]([CH2:23][CH2:22][CH2:21][C:20]#[CH:19])[C:6]2=[N:7][CH:8]=1)=[O:11])[CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 110197205-Iodo-1-pentyneHCID 14590535CID 14590535

生成物 1

HCID 20139384Ethyl-4-ethoxy-1-(pent-4-ynyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate収率 111.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

A mixture of 3.78 g of ethyl 4-ethoxy-1H-pyrazolo-[3,4-b]pyridine-5-carboxylate, 3.90 g of 1-iodo-4-pentyne, and 6.68 g of pulverized anhydrous potassium carbonate in 27 ml of dry DMF was stirred at 50°-60° for 1 hr. The mixture was cooled, poured into water, and the resulting mixture extracted with EtOAc. The combined extracts were washed with water and brine, dried (MgSO4), filtered, and concentrated to leave 5.42 g of a dark oil which slowly crystallized. This material was chromatographed over silica gel using EtOAc/hexane 1:2 (v/v) as the eluant to give 3.03 g (62%) of the title compound as a white solid. A small quantity was recrystallized from toluene to give white crystals, m.p. 84°-85.5°.

後処理

  1. temperatureThe mixture was cooled
  2. extractionthe resulting mixture extracted with EtOAc
  3. washThe combined extracts were washed with water and brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-f6bfb04c757b4e6fb17edb4ba061a7f5
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04745121

反応ノート

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