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

HRID 1281819
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HRID 1281819 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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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]benzodiazepine수율 82.9%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매
HCID 702
Ethanol
용매

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-8cb91432698e408f807595f845aa7913
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455521B1

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