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Iodine → HCID 178506564、化合物

HRID 2078718
ノート
印刷プレビュー

反応式

HRID 2078718 の反応式
[OH-].[K+].[C:3]1([C:9]2[S:16][C:15]3[CH:14]=[N:13][NH:12][C:11]=3[CH:10]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[I:17]I.OS([O-])=O.[Na+]>O.CN(C)C=O>[I:17][C:14]1[C:15]2[S:16][C:9]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=3)=[CH:10][C:11]=2[NH:12][N:13]=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 4

HCID 807IodineHCID 14797Potassium HydroxideHCID 23665763Sodium BisulfiteHCID 576373325-phenyl-1H-thieno[3,2-c]pyrazole2 回

生成物 1

HCID 178506564HCID 178506564、化合物収率 91.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒

実験手順

Crushed KOH (1.09 g, 6.49 mmol) was added in one portion to a stirred mixture of 5-phenyl-1H-thieno[3,2-c]pyrazole [1.30 g, 6.49 mmol, Intermediate (45)], iodine (2.47 g, 9.73 mmol), and dimethylformamide (15 mL) under nitrogen at room temperature and the dark reaction was stirred at room temperature. After 3 hours, 10% aqueous NaHSO3 (40 mL) was added with stirring. The resulting slurry was diluted with water (40 mL) and the mixture stirred at room temperature for 5 minutes. The solid was collected by filtration, washed three times with water (20 mL) and then dried under high vacuum at 40° C. to give 3-iodo-5-phenyl-1H-thieno[3,2-c]pyrazole [1.94 g 91%, Intermediate (46)] as a tan powder. TLC Rf 0.52 (silica, 70% ethyl acetate/heptane); LC/MS: 326.94 (M+H), RT=3.38 minutes; 1H NMR [600 Mhz, (CD3)2SO]: δ 13.51 (br s 1H), 7.73 (m, 2H), 7.69 (br s, 1H), 7.46 (m, 2H), 7.38 (m, 1 Hz).

後処理

  1. customthe dark reaction
  2. stirringwith stirring
  3. stirringthe mixture stirred at room temperature for 5 minutes
  4. filtrationThe solid was collected by filtration
  5. washwashed three times with water (20 mL)
  6. customdried under high vacuum at 40° C.

出典と根拠

ORDレコード
ord-1bb3bb09024e42128eeab6392c9319ef
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07928231B2

反応ノート

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