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Acetic Acid → 4-({[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzonitrile

HRID 2089685
ノート
印刷プレビュー

反応式

HRID 2089685 の反応式
COC(=O)[O:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[C:10]([C:16](=[N:29][C:30]2[CH:35]=[CH:34][C:33]([C:36]#[N:37])=[CH:32][CH:31]=2)[C:17]2[NH:21][C:20](=[O:22])[N:19]([C:23]3[N:28]=[CH:27][CH:26]=[CH:25][N:24]=3)[N:18]=2)[C:9]=1[F:38].C([BH3-])#N.[Na+].C(O)(=O)C.[OH-].[Na+]>O.O1CCCC1.CO>[F:38][C:9]1[C:8]([O:7][CH2:6][CH2:5][OH:4])=[CH:13][C:12]([O:14][CH3:15])=[CH:11][C:10]=1[CH:16]([NH:29][C:30]1[CH:31]=[CH:32][C:33]([C:36]#[N:37])=[CH:34][CH:35]=1)[C:17]1[NH:21][C:20](=[O:22])[N:19]([C:23]2[N:24]=[CH:25][CH:26]=[CH:27][N:28]=2)[N:18]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 176Acetic Acid2 回HCID 14798Sodium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 136334031Carbonic acid 2-{3-[(4-cyanophenylimino)-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]-2-fluoro-5-methoxyphenoxy}ethyl ester methyl ester

生成物 1

HCID 135982076
4-({[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzonitrile
収率 93.8%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
15 °C

実験手順

A suspension of carbonic acid 2-{3-[(4-cyanophenylimino)-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]-2-fluoro-5-methoxyphenoxy}ethyl ester methyl ester (25.0 g, 47.1 mmol) and methanol (90 mL) was cooled to 15° C. Sodium cyanoborohydride (5.45 g, 87 mmol) was added thereto, and was rinsed with methanol (10 mL). Acetic acid (21.5 mL, 375 mmol) was added dropwise thereto, and the resulting mixture was stirred at room temperature for 28 hours. The mixture was cooled in an ice-water bath, and tetrahydrofuran (100 mL) and a 5 N aqueous sodium hydroxide solution (113 mL, 565 mmol) were added thereto. After stirring the resulting mixture for 18 hours, the mixture was cooled to 15° C. or below, and acetic acid (81 mL, 1.410 mol) was added thereto. To the solution obtained, a seed crystal (5.0 mg) of the captioned compound was added at room temperature, and water (250 mL) was added dropwise to the resulting mixture, after which the resulting mixture was stirred at 4° C. for 21.5 hours. The suspension obtained was filtered and was washed with 25% aqueous methanol (100 mL) and dried at 40° C. under reduced pressure to obtain the captioned compound (21.1 g) as a white solid.

後処理

  1. washwas rinsed with methanol (10 mL)
  2. temperatureThe mixture was cooled in an ice-water bath
  3. stirringAfter stirring the resulting mixture for 18 hours
  4. temperaturethe mixture was cooled to 15° C. or below
  5. customTo the solution obtained
  6. stirringafter which the resulting mixture was stirred at 4° C. for 21.5 hours
  7. customThe suspension obtained
  8. filtrationwas filtered
  9. washwas washed with 25% aqueous methanol (100 mL)
  10. customdried at 40° C. under reduced pressure

出典と根拠

ORDレコード
ord-e9fef781901d462c8c180cccbb6bfc5a
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08436009B2

反応ノート

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