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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 5-Chloroisoquinoline-4-carboxylic acid

HRID 1470505
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HRID 1470505 반응식
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([C:12]([O:14]C)=[O:13])=[CH:5][N:6]=[CH:7]2.[OH-].[K+].Cl>CO.O>[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[C:4]([C:12]([OH:14])=[O:13])=[CH:5][N:6]=[CH:7]2
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 68281881Methyl 5-chloroisoquinolin-4-carboxylate

생성물 1

HCID 682819645-Chloroisoquinoline-4-carboxylic acid

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매2회

실험 절차

To a stirred solution of methyl 5-chloroisoquinolin-4-carboxylate (Intermediate-42) (3.8 g, 17.1 mmol) in MeOH (30 mL) was added, KOH (9.62 g, 171 mmol) solution in H2O (20 mL) and the reaction mixture was heated to 70° C. for 3 h. After completion (TLC), it was concentrated under vacuum to give crude product (3.5 g) that was diluted with water, acidified with 1N HCl (pH=3) and the aqueous phase was extracted with EtOAc, dried and concentrated under vacuum to afford the desired acid derivative (3 g, 84%) as an off white solid.

후처리

  1. concentrationAfter completion (TLC), it was concentrated under vacuum
  2. customto give crude product (3.5 g) that
  3. extractionthe aqueous phase was extracted with EtOAc
  4. customdried
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-1cecb7aa22be4b98b26767766448b1a9
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006442B2

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