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Hydrochloric Acid → 5-Amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one

HRID 490560
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HRID 490560 반응식
[Cl:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([N+:16]([O-])=O)=[CH:13][CH:14]=3)[C:9](=[O:19])[NH:8]2)=[CH:4][CH:3]=1.Cl.Cl[Sn]Cl.C(=O)(O)[O-].[Na+]>>[NH2:16][C:12]1[CH:11]=[C:10]2[C:15](=[CH:14][CH:13]=1)[N:7]([CH2:6][C:5]1[CH:20]=[CH:21][C:2]([Cl:1])=[CH:3][CH:4]=1)[NH:8][C:9]2=[O:19]
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 24479Stannous ChlorideHCID 516892Sodium BicarbonateHCID 68833180HCID 68833180, 화합물

생성물 1

HCID 105642105-Amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one수율 76.4%

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온도
85 °C

실험 절차

To 1-(4-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-one (0.45 g) was added HCl (37% aq.) solution (5 mL) followed by SnCl2.dihydrate (1.9 g). The mixture was heated to 85° C. for one hour. The reaction was then neutralized with sodium bicarbonate solution, filtered, and the filtrate extracted with EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and reduced in vacuo. Flash column chromatography of the residue over silica gel eluting with methylene chloride/methanol afforded the desired 5-amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one (0.31 g) as a dark brown solid. MS (ESI+): 274.4 [M+H]+).

후처리

  1. filtrationfiltered
  2. extractionthe filtrate extracted with EtOAc
  3. washThe combined organic phases were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-bae5617fcf07438d8df71446bcf95b0b
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07528158B2

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