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Hydrochloric Acid → 5-(3-Piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic Acid Hydrochloride

HRID 1437687
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HRID 1437687 반응식
C([O:3][C:4]([C:6]1[NH:24][C:9]2=[N:10][CH:11]=[C:12]([O:14][CH2:15][CH2:16][CH2:17][N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[CH:13]=[C:8]2[CH:7]=1)=[O:5])C.[ClH:25]>O1CCOCC1>[ClH:25].[N:18]1([CH2:17][CH2:16][CH2:15][O:14][C:12]2[CH:13]=[C:8]3[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[NH:24][C:9]3=[N:10][CH:11]=2)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 684241025-(3-Piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic Acid Ethyl Ester

생성물 1

HCID 684243705-(3-Piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic Acid Hydrochloride수율 100%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To the solution of 0.18 g (0.54 mmol) 5-(3-piperidin-1-yl-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid ethyl ester in 1.2 ml dioxan, 0.54 ml (0.64 g) concentrated hydrochloric acid were added. The reaction mixture was heated under reflux for 18 h, evaporated and dried under high vacuum over phosphorus pentoxide to give 0.18 g (100%) of the compound as a light brown solid.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for 18 h
  3. customevaporated
  4. dry with materialdried under high vacuum over phosphorus pentoxide

출처 및 근거

ORD 기록
ord-70f5636dc917483e8f920839aefdb9f2
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07622466B2

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