홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1-(4-Fluorophenyl)piperazine → HCID 59833503, 화합물

HRID 1443895
노트
인쇄 미리보기

반응식

HRID 1443895 반응식
F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.C(N(C(C)C)CC)(C)C.[F:32][C:33]1[CH:38]=[CH:37][C:36]([N:39]2[CH2:44][CH2:43][NH:42][CH2:41][CH2:40]2)=[CH:35][CH:34]=1.[O:45]=[C:46]1[C:55]2[C:50](=[CH:51][CH:52]=[CH:53][CH:54]=2)[C:49]([CH2:56][C:57]2[CH:58]=[C:59]([CH:63]=[CH:64][CH:65]=2)[C:60](O)=[O:61])=[N:48][NH:47]1>CC(N(C)C)=O.O>[F:32][C:33]1[CH:34]=[CH:35][C:36]([N:39]2[CH2:44][CH2:43][N:42]([C:60]([C:59]3[CH:58]=[C:57]([CH:65]=[CH:64][CH:63]=3)[CH2:56][C:49]3[C:50]4[C:55](=[CH:54][CH:53]=[CH:52][CH:51]=4)[C:46](=[O:45])[NH:47][N:48]=3)=[O:61])[CH2:41][CH2:40]2)=[CH:37][CH:38]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 752601-(4-Fluorophenyl)piperazineHCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 251319063-((4-Oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoic acid

생성물 1

HCID 59833503HCID 59833503, 화합물수율 47.7%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 31374Dimethylacetamide용매

실험 절차

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (150 mg, 0.47 mmol), diisopropylethylamine (102 mg, 0.8 mmol) and 1-(4-fluorophenyl)piperazine (65 mg, 0.47 mmol) were added sequentially at ambient temperature to a stirred solution of 3-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)benzoic acid (A)(100 mg, 0.36 mmol) in dry dimethylacetamide (1 ml), the mixture was stirred at ambient temperature for 4 hours and allowed to stand at ambient temperature for 16 hours, then it was added dropwise to stirred cold water (10 ml). After 30 minutes, the resulting solid was collected by filtration, washed with water (2×1 ml) and hexane (1 ml), dried in vacuo and purified using preparative HPLC to give 4-{3-[4-(4-fluorophenyl)piperazin-1-ylcarbonyl]benzyl}-1(2H)-phthalazinone (21)(76 mg) as a cream solid; m/z (M+H)+. 443; HPLC Purity 90%; HPLC Retention time 4.00 minutes.

후처리

  1. waitto stand at ambient temperature for 16 hours
  2. additionit was added dropwise
  3. waitAfter 30 minutes
  4. filtrationthe resulting solid was collected by filtration
  5. washwashed with water (2×1 ml) and hexane (1 ml)
  6. customdried in vacuo
  7. custompurified

출처 및 근거

ORD 기록
ord-579ec8b2eb584178bb5ac9d7f4680ad9
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07662818B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트