摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

BOC-(R)-3-氨基-4-(3,4-二氟苯基)丁酸 | 269396-59-0

中文名称
BOC-(R)-3-氨基-4-(3,4-二氟苯基)丁酸
中文别名
Boc-D-3-氨基-4-(3,4-二氟苯基)丁酸;(3R)-3-[(叔丁氧羰基)氨基]-4-(3,4-二氟苯基)丁酸;BOC-D-Β-3-氨基-4-(3,4-二氟苯基)-丁酸
英文名称
(3R)-3-[(1,1-dimethylethoxycarbonyl)amino]-4-(3,4-difluorophenyl)butanoic acid
英文别名
(R)-3-(tert-butoxycarbonylamino)-4-(3,4-difluorophenyl)butanoic acid;3-(R)-t-butyloxycarbonylamino-4-(3,4-difluorophenyl)butyric acid;(R)-3-((tert-butoxycarbonyl)amino)-4-(3,4-difluorophenyl)butanoic acid;(3R)-4-(3,4-difluorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
BOC-(R)-3-氨基-4-(3,4-二氟苯基)丁酸化学式
CAS
269396-59-0
化学式
C15H19F2NO4
mdl
MFCD01860952
分子量
315.317
InChiKey
XZGBRONJONQTTA-SNVBAGLBSA-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:
    448.6±45.0 °C(Predicted)
  • 密度:
    1.243

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.466
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    6

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2924299090
  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P330,P363,P501
  • 危险性描述:
    H302,H312,H332
  • 储存条件:
    存储条件:2-8℃,请保持干燥。

SDS

SDS:d2bfef510677d125b40b0ef8707d28b9
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    BOC-(R)-3-氨基-4-(3,4-二氟苯基)丁酸 在 lithium hydroxide 、 1-羟基苯并三唑1-(3-二甲基氨基丙基)-3-乙基碳二亚胺N,N-二异丙基乙胺 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 生成 (S)-1-[(R)-3-tert-Butoxycarbonylamino-4-(3,4-difluoro-phenyl)-butyryl]-pyrrolidine-2-carboxylic acid
    参考文献:
    名称:
    有效和选择性脯氨酸衍生的二肽基肽酶IV抑制剂。
    摘要:
    对Merck样品的内部筛选表明,脯氨酸衍生的高苯丙氨酸3作为DPP-IV抑制剂具有中等效力(DPP-IV IC50 = 1.9 microM)。对3的优化导致化合物37,它是迄今为止发现的最有效和选择性最强的DPP-IV抑制剂之一。
    DOI:
    10.1016/j.bmcl.2004.07.056
  • 作为产物:
    描述:
    参考文献:
    名称:
    发现有效的和选择性的基于β-高苯丙氨酸的二肽基肽酶IV抑制剂。
    摘要:
    内部筛选铅β-氨基酰基脯氨酸8的修饰得到了等价的噻唑烷化物9。对9的苯环的广泛SAR研究导致发现了一系列新的有效的和选择性的DP-IV抑制剂。事实证明,在2位上引入氟对于该系列的效能至关重要。2,5-二氟(22q)和2,4,5-三氟(22t)类似物是DP-IV的有效抑制剂(分别为IC(50)= 270、119nM)。
    DOI:
    10.1016/j.bmcl.2004.06.099
点击查看最新优质反应信息

文献信息

  • BETA-AMINO HETEROCYCLIC DIPEPTIDYL PEPTIDASE INHIBITORS FOR THE TREATMENT OR PREVENTION OF DIABETES
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20150359793A1
    公开(公告)日:2015-12-17
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    本发明涉及一种抑制二肽基肽酶-IV酶(“DP-IV抑制剂”)的化合物,该化合物在治疗或预防二肽基肽酶-IV酶参与的疾病中具有用途,如糖尿病,特别是2型糖尿病。该发明还涉及包含这些化合物的药物组合物,以及在预防或治疗二肽基肽酶-IV酶参与的这类疾病中使用这些化合物和组合物。
  • Beta-amino tetrahydroimidazo (1, 2-a) pyrazines and tetrahydrotrioazolo (4,3-a) pyrazines as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
    申请人:——
    公开号:US20040167133A1
    公开(公告)日:2004-08-26
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    本发明涉及一种抑制二肽基肽酶-IV酶(“DP-IV抑制剂”)的化合物,该化合物对于治疗或预防二肽基肽酶-IV酶参与的疾病,如糖尿病,特别是2型糖尿病非常有用。本发明还涉及包含这些化合物的制药组合物,以及使用这些化合物和组合物预防或治疗二肽基肽酶-IV酶参与的疾病的方法。
  • NOVEL CYCLIC AZABENZIMIDAZOLE DERIVATIVES USEFUL AS ANTI-DIABETIC AGENTS
    申请人:Edmondson Scott D.
    公开号:US20110190308A1
    公开(公告)日:2011-08-04
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    本发明涉及抑制二肽基肽酶-IV酶(“DP-IV抑制剂”)的化合物,这些化合物可用于治疗或预防涉及二肽基肽酶-IV酶的疾病,例如糖尿病,特别是2型糖尿病。本发明还涉及包括这些化合物的制药组合物以及在涉及二肽基肽酶-IV酶的这些疾病的预防或治疗中使用这些化合物和组合物。
  • [EN] BETA-AMINO TETRAHYDROIMIDAZO (1, 2-A) PYRAZINES AND TETRAHYDROTRIOAZOLO (4, 3-A) PYRAZINES AS DIPEPTIDYL PEPTIDASE INHIBITORS FOR THE TREATMENT OR PREVENTION OF DIABETES<br/>[FR] PYRAZINES BETA-AMINO TETRAHYDROIMIDAZO (1, 2-A) ET PYRAZINES TETRAHYDROTRIOAZOLO (4, 3-A) UTILISEES EN TANT QU'INHIBITEURS DE LA DIPEPTIDYL PEPTIDASE DANS LE TRAITEMENT OU LA PREVENTION DU DIABETE
    申请人:MERCK & CO INC
    公开号:WO2003004498A1
    公开(公告)日:2003-01-16
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme ('DP-IV inhibitors') and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    本发明涉及一种抑制二肽基肽酶-IV酶(“DP-IV抑制剂”)的化合物,该化合物可用于治疗或预防二肽基肽酶-IV酶参与的疾病,例如糖尿病,特别是2型糖尿病。本发明还涉及包含这些化合物的制药组合物以及在预防或治疗二肽基肽酶-IV酶参与的这些疾病中使用这些化合物和组合物。
  • Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
    申请人:——
    公开号:US20030100563A1
    公开(公告)日:2003-05-29
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    本发明涉及抑制二肽基肽酶-IV酶(“DP-IV抑制剂”)的化合物,这些化合物在治疗或预防二肽基肽酶-IV酶参与的疾病,如糖尿病,尤其是2型糖尿病方面具有用途。本发明还涉及包含这些化合物的制药组合物以及在预防或治疗二肽基肽酶-IV酶参与的这些疾病中使用这些化合物和组合物的用途。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐