Tivozanib

Tivozanib 구조식 이미지
카스 번호:
475108-18-0
상품명:
Tivozanib
동의어(영문):
AV951;CS-8;AV-951;KRN-951;Tivozanib;TIVOZANIB;AV951;AV-951(Tivozanib);Tivozanib USP/EP/BP;Tivozanib(AV951,KRN951);Lactic Acid Impurity 21
CBNumber:
CB82484655
분자식:
C22H19ClN4O5
포뮬러 무게:
454.86
MOL 파일:
475108-18-0.mol
MSDS 파일:
SDS

Tivozanib 속성

녹는점
>202°C (dec.)
끓는 점
550.4±50.0 °C(Predicted)
밀도
1.421
저장 조건
Refrigerator
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨, 가열)
물리적 상태
백색 분말.
산도 계수 (pKa)
11.74±0.70(Predicted)
색상
페일베이지부터 라이트브라운까지

안전

Tivozanib C화학적 특성, 용도, 생산

용도

Tivozanib also known as AV-951 is an orally bioavailable potent VEGFR-1, 2 and 3, c-Kit and PDGFR inhibitor with IC50 of 0.21, 0.16, 0.24, 1.63 and 1.72 nM, respectively.

Synthesis

The synthesis of Tivozanib is as follows:
Phenyl chlorocarbonate (601 g) was added dropwise to 3-amino-5-methylisoxazole (377 g), pyridine (1215 g), and N,N-dimethylacetamide (4 L) at 0°C, and the mixture was stirred at 20°C for 2 hr. 4-[(4-Amino-3-chlorophenol)oxy]-6,7-dimethoxyquinoline (847 g) was added to the reaction solution, and the mixture was stirred at 80°C for 5 hr. The reaction solution was cooled to 5°C. Thereafter, methanol (8.5 L) and water (8.5 L) were added thereto, and the mixture was neutralized with an aqueous sodium hydroxide solution. The resultant precipitate was collected by filtration, and the filtered product was slurried in water (8.5 L) for washing. The slurry was filtered, and the filtered product was then dried under the reduced pressure to give Tivozanib (1002 g, yield 86.1%).
synthesis of Tivozanib.png

Tivozanib 준비 용품 및 원자재

원자재

준비 용품


Tivozanib 공급 업체

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