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Hydrochloric Acid → 3-bromo-1-cyclopentyl-4-methoxy-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-7-carboxylic acid

HRID 2206045
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반응식

HRID 2206045 반응식
[Br:1][C:2]1[C:6]2[CH:7]([O:15][CH3:16])[NH:8][CH:9]=[C:10]([C:11]([O:13]C)=[O:12])[C:5]=2[N:4]([CH:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:3]=1.[OH-].[Na+].Cl>CO>[Br:1][C:2]1[C:6]2[CH:7]([O:15][CH3:16])[NH:8][CH:9]=[C:10]([C:11]([OH:13])=[O:12])[C:5]=2[N:4]([CH:17]2[CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:3]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 117987803methyl 3-bromo-1-cyclopentyl-4-methoxy-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-7-carboxylate

생성물 1

HCID 1179880413-bromo-1-cyclopentyl-4-methoxy-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-7-carboxylic acid수율 106.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methyl 3-bromo-1-cyclopentyl-4-methoxy-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-7-carboxylate (874 mg) in methanol (8 mL) was added 1N aqueous sodium hydroxide solution (8 mL), and the mixture was stirred at room temperature for 3 hr. To the reaction mixture was added 1N hydrochloric acid at 0° C., and the precipitate was collected by filtration, and dried to give the title compound (894 mg).

후처리

  1. filtrationthe precipitate was collected by filtration
  2. customdried

출처 및 근거

ORD 기록
ord-bb02cae836f34109975233a0c0ddded2
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371320B2

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