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

HRID 649953
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반응식

HRID 649953 반응식
[Sn](Cl)Cl.[F:4][C:5]1[CH:6]=[CH:7][C:8]2[C:12]([C:13]#[N:14])=[C:11]([NH:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[N+:22]([O-])=O)[S:10][C:9]=2[CH:25]=1.O>Cl.C(O)C>[NH2:14][C:13]1[C:12]2[C:8]3[CH:7]=[CH:6][C:5]([F:4])=[CH:25][C:9]=3[S:10][C:11]=2[NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[N:22]=1
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참가 물질

6

반응물 3

HCID 962WaterHCID 24479Stannous ChlorideHCID 184221416-Fluoro-2-(2-nitroanilino)benzo[b]thiophene-3-carbonitrile

생성물 1

HCID 13581640212-amino-3-fluoro-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

반응 조건

온도
50 °C

실험 절차

Tin(II) chloride (50 g) was dissolved in a 18% hydrochloric acid (250 ml) solution heated to 50° C., and a suspension of 6-fluoro-2-(2-nitroanilino)benzo[b]thiophene-3-carbonitrile (20 g) in ethanol (280 ml) was added. The mixture was refluxed under heating for 4 hours. Then, the reaction mixture was cooled to 40° C. and poured into water (1 L) and the mixture was stood still for 30 minutes. The precipitated crystals were filtered by suction and washed with water (500 ml) to give 12-amino-3-fluoro-6H-[1]benzothieno[2,3-b][1,5]benzodiazepine.1 hydrochloride (15 g).

후처리

  1. additionwas added
  2. temperatureThe mixture was refluxed
  3. temperatureunder heating for 4 hours
  4. temperatureThen, the reaction mixture was cooled to 40° C.
  5. filtrationThe precipitated crystals were filtered by suction
  6. washwashed with water (500 ml)

출처 및 근거

ORD 기록
ord-f94359bd81404aea8e59f99343368191
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271225B1

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