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N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-dimethylamino-3-pyridazineamine | 75842-06-7

中文名称
——
中文别名
——
英文名称
N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-dimethylamino-3-pyridazineamine
英文别名
6-N-(2,5-dimethylpyrrol-1-yl)-3-N,3-N-dimethylpyridazine-3,6-diamine
N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-dimethylamino-3-pyridazineamine化学式
CAS
75842-06-7
化学式
C12H17N5
mdl
——
分子量
231.3
InChiKey
JYKIDGOZMWJQHD-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    445.3±55.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    46
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2,5-己二酮(6-hydrazino-pyridazin-3-yl)-dimethyl-amine溶剂黄146 为溶剂, 反应 3.0h, 以50%的产率得到N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-dimethylamino-3-pyridazineamine
    参考文献:
    名称:
    Antihypertensives. N-1H-Pyrrol-1-yl-3-pyridazinamines
    摘要:
    The hypothesis that the side effects of hydralazine, such as mutagenicity and lupus erythematosus like syndrome, might be due to the NHNH2 group prompted us to incorporate part of this moiety into a pyrrole ring. Therefore, we prepared a series of N-1H-pyrrol-1-yl-3-pyridazinamines and a limited number of N-1H-pyrrol-1-yl-1-phthalazinamines by reaction of 3-hydrazinopyridazines and 1-hydrazinophthalazines with gamma-diketones. Most of these compounds, especially in the pyridazine series, showed moderate to strong antihypertensive activity in spontaneously hypertensive rats. The decrease in blood pressure generally had a slow onset after either oral or intravenous administration. N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-(4-morpholinyl)-3-pyridazinamine hydrochloride (30) (MDL 899) showed no mutagenic activity in several tests and is now in clinical trials in patients.
    DOI:
    10.1021/jm00374a024
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文献信息

  • N-Pyrrolyl-pyridazineamines and their use as antihypertensive agents
    申请人:Gruppo Lepetit S.p.A.
    公开号:US04247551A1
    公开(公告)日:1981-01-27
    New-pyrrolyl-3-pyridazineamines having a further aminic substituent in the position 6. The compounds are useful as antihypertensive agents and may be prepared from 6-amino substituted-3-hydrazino pyridazines and .beta.-dicarbonyl compounds. The use of the novel compounds as antihypertensives and compositions containing the novel compounds as active ingredients are also claimed.
    具有位置6进一步氨基取代物的新吡咯基-3-吡啶嗪胺类化合物。这些化合物可用作降压药物,并可从6-氨基取代-3-叠氮基吡啶嗪和β-二羰基化合物制备。还声称将这些新化合物用作降压药物,并含有这些新化合物作为活性成分的组合物。
  • 6-Amino substituted N-pyrrolyl-3-pyridazine amines, their preparation, and pharmaceutically antihypertensive compositions containing them
    申请人:GRUPPO LEPETIT S.P.A.
    公开号:EP0009655A1
    公开(公告)日:1980-04-16
    New N-pyrrolyl-3-pyridazine-amines having a further aminic substituent in the 6 position of the formula (I), wherein R, R1, R2 and R3 are hydrogen or lower alkyl, R4 is e.g hydrogen or lower alkyl, R5 and R6 are e.g. lower alkyl or taken together with the adjacent nitrogen atom represent a saturated 5 - 6 membered heterocyclic ring which may contain a further heteroatom, R7 and R8 represent hydrogen or, taken together, a 1,3-butadienylene radical forming a benzo system fused with the pyridazine ring, for example N-2,5-dimethyl-1H-pyrrol-1-yl)- 6-morpholino-3-pyridazineamine or N-(2,5-dimethyl-1H-pyrrol- 1-yl)-4-(4-hydroxypiperidino)-1-phthalazineamine, and their pharmaceutically acceptable salts are made e.g. by contacting a hydrazino derivate of the formula (II), wherein the substituents have the same meaning as above or an acid addition salt thereof with a dicarbonyl compound of the formula (III), wherein the substituents have the same meaning as above, or a functional derivative thereof in the presence of an acid catalyst at a temperature between 15°C and 120°C. The new compounds can be used as antihypertensive agents.
    在式 (I) 的 6 位具有另一个氨基取代基的新型 N-吡咯烷-3-哒嗪胺、 其中 R、R1、R2 和 R3 为氢或低级烷基,R4 如为氢或低级烷基,R5 和 R6 如为R5和R6是低级烷基,或与相邻的氮原子一起代表一个饱和的 5 - 6 个成员的杂环,该杂环可能含有另一个杂原子,R7和R8代表氢,或与 1、例如 N-2,5-二甲基-1H-吡咯-1-基)-6-吗啉基-3-哒嗪胺或 N-(2,5-二甲基-1H-吡咯-1-基)-4-(4-羟基哌啶基)-1-酞嗪胺及其药学上可接受的盐。例如,将式(II)的肼基衍生物(其中取代基的含义同上)或其酸加成盐与式 (III)的二羰基化合物(其中取代基的含义同上)或其官能衍生物在酸催化剂存在下于 15°C 至 120°C 的温度下接触。 新化合物可用作降压药。
  • US4247551A
    申请人:——
    公开号:US4247551A
    公开(公告)日:1981-01-27
  • Antihypertensives. N-1H-Pyrrol-1-yl-3-pyridazinamines
    作者:Elvio Bellasio、Ambrogio Campi、Nunzio Di Mola、Emiliana Baldoli
    DOI:10.1021/jm00374a024
    日期:1984.8
    The hypothesis that the side effects of hydralazine, such as mutagenicity and lupus erythematosus like syndrome, might be due to the NHNH2 group prompted us to incorporate part of this moiety into a pyrrole ring. Therefore, we prepared a series of N-1H-pyrrol-1-yl-3-pyridazinamines and a limited number of N-1H-pyrrol-1-yl-1-phthalazinamines by reaction of 3-hydrazinopyridazines and 1-hydrazinophthalazines with gamma-diketones. Most of these compounds, especially in the pyridazine series, showed moderate to strong antihypertensive activity in spontaneously hypertensive rats. The decrease in blood pressure generally had a slow onset after either oral or intravenous administration. N-(2,5-Dimethyl-1H-pyrrol-1-yl)-6-(4-morpholinyl)-3-pyridazinamine hydrochloride (30) (MDL 899) showed no mutagenic activity in several tests and is now in clinical trials in patients.
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