2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile

2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile 구조식 이미지
카스 번호:
1187595-85-2
상품명:
2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile
동의어(영문):
2-[1-(Ethylsulfonyl)-3-azetidinylidene]acetonitrile;Baricitinib-010;Baricitinib Intermediates;Baricitinib intermediate 2;[1-(ethylsulfonyl)azetidin-3-ylidene]acetonitrile;2-(1-ETHYLSULFONY)AZETIDIN-3-YLIDENE)ACETONITRILE;(1-Ethanesulfonyl-azetidin-3-ylidene)-acetonitrile;2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile;2-[1-(ethanesulfonyl)azetidin-3-ylidene]acetonitrile;2-[1-(ethyl sulfonyl) -3-azacyclobutyl] acetonitrile
CBNumber:
CB62715957
분자식:
C7H10N2O2S
포뮬러 무게:
186.23
MOL 파일:
1187595-85-2.mol

2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile 속성

녹는점
67-69°C
끓는 점
360.8±52.0 °C(Predicted)
밀도
1.33±0.1 g/cm3(Predicted)
저장 조건
Sealed in dry,Room Temperature
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
-8.49±0.20(Predicted)
물리적 상태
고체
물리적 상태
단단한 모양
색상
황백색에서 밝은 노란색까지
InChI
InChI=1S/C7H10N2O2S/c1-2-12(10,11)9-5-7(6-9)3-4-8/h3H,2,5-6H2,1H3
InChIKey
HQUIOHSYUKWGOM-UHFFFAOYSA-N
SMILES
C(#N)/C=C1\CN(S(CC)(=O)=O)C\1
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
HS 번호 2933998090
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.

2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile C화학적 특성, 용도, 생산

용도

2-(1-(Ethylsulfonyl)azetidin-3-ylidene)acetonitrile is an intermediate in the synthesis of Baricitinib, a JAK 1 and 2 inhibitor used in the treatment of rheumatoid arthritis.

Synthesis

2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile is synthesized by first treating azetidine-3-ol hydrochloride with an equimolar equivalent of an alkanesulfonyl chloride, preferably ethanesulfonyl chloride, to give l-ethylsulfonylazetidin-3-ol. Preferably, the reaction is performed in a biphasic solution comprising a mixture of an organic phase and a aqueous phase, preferably THF with an aqueous solution which is basic, while maintaining the solution at room temperature or a temperature slightly below room temperature, preferably 20 °C. The reaction is followed to completion using standard monitoring techniques. Typically, the reaction is complete within 1 to 5 hours. The organic layer is removed, preferably by distillation, and the aqueous layer is extracted with an appropriate solvent such as toluene, p-cymene, and CPME. Preferably the extraction solvent is toluene. Alternatively, the toluene extractions can be excluded if recrystallization of 2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile is performed.

synthesis route of 2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile

2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile 준비 용품 및 원자재

원자재

준비 용품


2-(1-(ethylsulfonyl)azetidin-3-ylidene)acetonitrile 공급 업체

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Shanghai Jinli Pharmaceutical Co.,Ltd
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Jinan Million Pharmaceutical Co., Ltd
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Hangzhou ICH Biofarm Co., Ltd
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Beijing Cooperate Pharmaceutical Co.,Ltd
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Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
ATK CHEMICAL COMPANY LIMITED
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career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Shanghai Arbor Chemical Co., Ltd.
021-60451682
act@arborchemical.com CHINA 906 58

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