1-에틸-1H-피라졸-4-아민

1-에틸-1H-피라졸-4-아민
1-에틸-1H-피라졸-4-아민 구조식 이미지
카스 번호:
876343-24-7
한글명:
1-에틸-1H-피라졸-4-아민
동의어(한글):
1-에틸-1H-피라졸-4-아민
상품명:
1-ethyl-1H-pyrazol-4-amine
동의어(영문):
1-ethylpyrazol-4-amine;4-Amino-1-ethylpyrazole;1-ethyl-1H-pyrazol-4-amine;4-Amino-1-ethyl-1H-pyrazole;1H-Pyrazol-4-amine, 1-ethyl-;1-ethyl-1H-pyrazol-4-amine hydrochloride;1-ethyl-1H-pyrazol-4-amine(SALTDATA: HCl)
CBNumber:
CB11532949
분자식:
C5H9N3
포뮬러 무게:
111.15
MOL 파일:
876343-24-7.mol

1-에틸-1H-피라졸-4-아민 속성

끓는 점
238.6±13.0 °C(Predicted)
밀도
1.16±0.1 g/cm3(Predicted)
저장 조건
under inert gas (nitrogen or Argon) at 2–8 °C
산도 계수 (pKa)
3.72±0.10(Predicted)
CAS 데이터베이스
876343-24-7
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험 등급 IRRITANT
HS 번호 2933199090
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:
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P312 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.

1-에틸-1H-피라졸-4-아민 C화학적 특성, 용도, 생산

용도

1-ethyl-1H-pyrazol-4-amine can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Synthesis

Synthesis_876343-24-7
General Procedure for the Synthesis of 4-Amino-l-N-alkylated-pyrazolesA solution of 4-nitropyrazole (300mg, 2.65mmol), potassium carbonate (2eq) and the alkylating reagent (l .leq) in acetonitrile (lOmL) was heated at 60??C for 18h. After cooling to rt the mixture was diluted with EtOAc and washed with water. The organic phase was collected, dried (MgS04) and concentrated in vacuo. The crude residue was dissolved in methanol (lOmL), palladium on carbon (50mg) was added and the reaction was stirred under a balloon of hydrogen for 18h. The resulting mixture was filtered through Celite and the filtrate concentrated in vacuo to give the desired product. Procedure B:Example 11: 2-((6-( 1 -Ethyl- 1 H-pyrazo 1-4-ylamino)- 1 H-pyrazo lo [3 ,4-d]pyrimidin- 1 -yl) methyl)benzonitrileThe following compound was made according to the procedure in Example 1, using 1-ethyl- lH-pyrazo 1-4-amine. 1 -ethyl- lH-pyrazol-4-amine was prepared by Procedure A using ethyl iodide as alkylating agent: 1H NMR (d6-DMSO) |? 9.94 (s, 1H), 8.94 (s, 1H), 8.10 (s, 2H), 7.91 (dd, 1H), 7.66 (td, 1H), 7.49-7.53 (m, 2H), 7.35-7.37 (m, 1H), 5.76 (s, 2H), 4.11 (q, 2H), 1.35 (t, 3H); LC-MS method B, (ES+) 345.1, RT = 8.58min.

1-에틸-1H-피라졸-4-아민 준비 용품 및 원자재

원자재

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