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Hydrochloric Acid → 12-amino-8-fluoro-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine

HRID 1281818
ノート
印刷プレビュー

反応式

HRID 1281818 の反応式
[NH2:1][C:2]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:3]=1[NH:4][C:5]1[S:9][C:8]2[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=2[C:6]=1[C:14]#[N:15].Cl>CO.O>[NH2:15][C:14]1[C:6]2[C:7]3[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=3[S:9][C:5]=2[NH:4][C:3]2[CH:16]=[C:17]([F:20])[CH:18]=[CH:19][C:2]=2[N:1]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 184222672-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile

生成物 1

HCID 1842238512-amino-8-fluoro-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

2-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile (155 g) was suspended in a mixture of methanol (250 ml) and water (200 ml) and 35% aqueous hydrochloric acid (42 ml) was added. The mixture was stirred under reflux with heating for 5.5 hours. The reaction mixture was cooled and stirred at 20° C. for 1 hour. The precipitated crystals were filtered by suction, washed successsively with water (500 ml) and isopropyl alcohol (200 ml) and dried in a drying box overnight to give 12-amino-8-fluoro-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine.1 hydrochloride (104 g) as yellow crystals.

後処理

  1. additionwas added
  2. temperatureunder reflux
  3. temperaturewith heating for 5.5 hours
  4. temperatureThe reaction mixture was cooled
  5. stirringstirred at 20° C. for 1 hour
  6. filtrationThe precipitated crystals were filtered by suction
  7. washwashed successsively with water (500 ml) and isopropyl alcohol (200 ml)
  8. customdried in a drying box overnight

出典と根拠

ORDレコード
ord-2c894e87d1114624adea2ec0303ac00b
出典データセット
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06455521B1

反応ノート

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