Sodium Chloride → HCID 20186089, 화합물

HRID 2309245노트

반응식

HRID 2309245 반응식
[Cl:1][C:2]1[CH:25]=[CH:24][C:5]([C:6]([NH:8][CH:9]([CH2:13][CH:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][C:15]2=O)[C:10]([OH:12])=[O:11])=[O:7])=[CH:4][CH:3]=1.[NH2-].[Na+].[CH2:28](Cl)[CH:29]=[CH2:30].[Cl-].[Na+].CN(C)C=[O:37]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:8][CH:9]([CH2:13][C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([O:37][CH2:28][CH:29]=[CH2:30])[CH:15]=2)[C:10]([OH:12])=[O:11])=[O:7])=[CH:24][CH:25]=1

참가 물질

6

반응물 5

HCID 5234Sodium ChlorideHCID 6228DimethylformamideHCID 7850Allyl chlorideHCID 24533Sodium amideHCID 13393254HCID 13393254, 화합물

생성물 1

HCID 20186089HCID 20186089, 화합물

실험 절차

479 Milligrams of 2-(4-chlorobenzoylamino)-3-(oxindol-3-yl)propionic acid 1/4-hydrate prepared in Example 3 and 0.05 g of sodium amide were admixed in 5 ml of dimethylformamide, and the mixture was stirred at a room temperature for 2 hours. Then 0.17 g of allyl chloride was added to the mixture and the resulting reaction mixture was stirred at a room temperature for 10 hours. The reaction mixture was poured into 13 ml of a saturated sodium chloride aqueous solution, and the organic material was extracted with chloroform. The chloroform layer was washed with water, dried, then chloroform was removed by evaporation. The residure thus obtained was purified by means of a silica gel column chromatography to yield 85 mg of 2-(4-chlorobenzoylamino)-3-(1-allyloxyindol-3-yl)propionic acid.

후처리

  1. customthe resulting reaction mixture
  2. stirringwas stirred at a room temperature for 10 hours
  3. extractionthe organic material was extracted with chloroform
  4. washThe chloroform layer was washed with water
  5. customdried
  6. customchloroform was removed by evaporation
  7. customThe residure thus obtained
  8. customwas purified by means of a silica gel column chromatography

출처 및 근거

ORD 기록
ord-9515d0a1b4914cecab75dcf208c2d7cc
출처 데이터셋
uspto-grants-1987_09
특허 번호
US04694017

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