Hydrochloric Acid → HCID 178487512, 화합물

HRID 651599

반응식

HRID 651599 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH2:12][N:13]3[CH2:17][CH2:16][C@H:15]([NH:18][S:19]([C:22]4[CH:31]=[CH:30][C:29]5[C:24](=[CH:25][C:26]([O:32][CH3:33])=[CH:27][CH:28]=5)[CH:23]=4)(=[O:21])=[O:20])[C:14]3=[O:34])[CH:10]=2)[CH:5]=[CH:4][N:3]=1.[OH-:35].[Na+].Cl>O1CCOCC1>[OH:35][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH2:12][N:13]3[CH2:17][CH2:16][CH:15]([NH:18][S:19]([C:22]4[CH:31]=[CH:30][C:29]5[C:24](=[CH:25][C:26]([O:32][CH3:33])=[CH:27][CH:28]=5)[CH:23]=4)(=[O:21])=[O:20])[C:14]3=[O:34])[CH:10]=2)[CH:5]=[CH:4][N:3]=1

참가 물질

5

실험 절차

7-Methoxynaphthalene-2-sulfonic acid [1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]amide (0.07 g, 0.14 mmol), prepared as described in EXAMPLE 1, Part K, is treated with dioxane (1 mL) and 10% aq. NaOH (3 mL) and heated to reflux for 48 hours. The reaction was cooled, acidified with 1 N HCl and extracted with CH2Cl2. The organic layer is separated, dried and concentrated. The residue is purified by column chromatography eluting with 2.5% MeOH/CH2Cl2. The product fractions are collected, concentrated and precipitated with dilute HCl/ether to yield the title compound (0.041 g, 0.086 mmol).

후처리

  1. temperatureheated
  2. temperatureto reflux for 48 hours
  3. temperatureThe reaction was cooled
  4. extractionextracted with CH2Cl2
  5. customThe organic layer is separated
  6. customdried
  7. concentrationconcentrated
  8. customThe residue is purified by column chromatography
  9. washeluting with 2.5% MeOH/CH2Cl2
  10. customThe product fractions are collected
  11. concentrationconcentrated
  12. customprecipitated with dilute HCl/ether

출처 및 근거

ORD 기록
ord-909cad4e41604bd6ab20d4d1fb720db6
출처 데이터셋
uspto-grants-2001_08
특허 번호
US06281227B1

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