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Sodium Bicarbonate → HCID 178433846、化合物

HRID 384332
ノート
印刷プレビュー

反応式

HRID 384332 の反応式
Cl.[NH2:2][C:3]1[C:4]([OH:19])=[C:5]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([OH:18])=[O:17])[CH:11]=2)[CH:6]=[C:7]([F:9])[CH:8]=1.[N:20]([O-])=O.[Na+].[O:24]1[C:28]2[CH:29]=[CH:30][C:31]([N:33]3[C:37](=[O:38])[CH2:36][C:35]([CH3:39])=[N:34]3)=[CH:32][C:27]=2[CH2:26][CH2:25]1.C(=O)(O)[O-].[Na+]>Cl>[O:24]1[C:28]2[CH:29]=[CH:30][C:31]([N:33]3[C:37](=[O:38])[C:36](=[N:20][NH:2][C:3]4[C:4]([OH:19])=[C:5]([C:10]5[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([OH:18])=[O:17])[CH:11]=5)[CH:6]=[C:7]([F:9])[CH:8]=4)[C:35]([CH3:39])=[N:34]3)=[CH:32][C:27]=2[CH2:26][CH2:25]1
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 516892Sodium BicarbonateHCID 23668193Sodium NitriteHCID 574837812-(2,3-Dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 574838163'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid hydrochloride

生成物 1

HCID 178433846HCID 178433846、化合物収率 20%

試薬・触媒・溶媒 1

HCID 313
Hydrochloric Acid
溶媒

実験手順

3′-Amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid hydrochloride 2f (219 mg, 0.772 mmol) was dissolved in 3 mL of hydrochloric acid (1 N) upon cooling by an ice-water bath, followed by dropwise addition of 1 mL of aqueous sodium nitrite (59 mg, 0.85 mmol). After the mixture was stirred for 20 minutes, 2-(2,3-dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 7c (150 mg, 0.69 mmol) was added. The mixture was adjusted to pH 8˜9 by batch addition of aqueous sodium bicarbonate (1.007 g, 11.57 mmol). The generated bubbles were quenched with 2 mL of ethanol. The reaction mixture was warmed up to room temperature and reacted overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was dissolved in 15 mL of water. After mixing well, the mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid, filtered and dried. The crude product was purified by HPLC to obtain the title compound 3′-{N′-[1-(2,3-dihydro-benzofuran-5-yl)-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 14 (65 mg, yield 20.0%) as a red solid.

後処理

  1. temperatureupon cooling by an ice-water bath
  2. customThe generated bubbles were quenched with 2 mL of ethanol
  3. customreacted overnight
  4. filtrationThe mixture was filtered
  5. dissolutionthe filter cake was dissolved in 15 mL of water
  6. additionAfter mixing well
  7. filtrationfiltered
  8. customdried
  9. customThe crude product was purified by HPLC

出典と根拠

ORDレコード
ord-d6decd527a0c41c09fd28a9586f7e539
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367710B2

反応ノート

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