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Stannous Chloride → methyl 7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate

HRID 715955
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반응식

HRID 715955 반응식
[N+:1]([C:4]1[CH:12]=[CH:11][C:10]2[N:9]3[CH2:13][CH2:14][CH2:15][C:8]3=[CH:7][C:6]=2[C:5]=1[C:16]([O:18][CH3:19])=[O:17])([O-])=O.[Sn](Cl)Cl>CO.O.C(Cl)Cl>[NH2:1][C:4]1[CH:12]=[CH:11][C:10]2[N:9]3[CH2:13][CH2:14][CH2:15][C:8]3=[CH:7][C:6]=2[C:5]=1[C:16]([O:18][CH3:19])=[O:17]
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참가 물질

6

반응물 2

HCID 24479Stannous ChlorideHCID 70984130methyl 7-nitro-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate2회

생성물 1

HCID 86712114methyl 7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate수율 70.6%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매
HCID 6344
Dichloromethane
용매

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온도
60 °C

실험 절차

A mixture of methyl 7-nitro-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate (Intermediate 19, 0.160 g) and tin (II) chloride (0.520 g) in methanol (6 mL) and water (0.06 mL) was heated at 60° C. for 8 hours. The resultant mixture was cooled and diluted with DCM and filtered through Celite. The filtrate was washed with 1M aqueous sodium hydroxide solution and brine, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo to give methyl 7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate (0.100 g) as a brown solid.

후처리

  1. filtrationfiltered through Celite
  2. washThe filtrate was washed with 1M aqueous sodium hydroxide solution and brine
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-d7380e5f0baf49fb98ffb9f9b61fced8
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187494B2

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