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

3-氨基-2,3-二氢螺[茚-1,4’-哌啶]-1’-羧酸叔丁酯 | 185527-11-1

中文名称
3-氨基-2,3-二氢螺[茚-1,4’-哌啶]-1’-羧酸叔丁酯
中文别名
3-氨基-2,3-二氢螺[茚-1,4'-哌啶]-1'-羧酸叔丁酯;3-氨基-2,3-二氢-1'H-螺[茚-1,4'-哌啶]-1'-羧酸叔丁酯
英文名称
3-amino-2,3-dihydrospiro[1H-indene-1,4'-piperidine]-1'-carboxylic acid 1,1-dimethylethyl ester
英文别名
tert-butyl 3-amino-2,3-dihydro-1'H-spiro[indene-1,4'-piperidine]-1'-carboxylate;tert-butyl 3-amino-2,3-dihydro-1'H-spiro[indene-1,4-piperidine]-1-carboxylate;Tert-butyl 3-amino-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate;tert-butyl 1-aminospiro[1,2-dihydroindene-3,4'-piperidine]-1'-carboxylate
3-氨基-2,3-二氢螺[茚-1,4’-哌啶]-1’-羧酸叔丁酯化学式
CAS
185527-11-1
化学式
C18H26N2O2
mdl
——
分子量
302.417
InChiKey
MRMIQWNSSBRSLQ-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:
    431.3±45.0 °C(Predicted)
  • 密度:
    1.14

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    55.6
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933399090
  • 储存条件:
    室温

SDS

SDS:25c97ae0197a60c4fa457a2bacb1883f
查看

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Spiro piperidines and homologs promote release of growth hormone
    申请人:Merck & Co., Inc.
    公开号:US05578593A1
    公开(公告)日:1996-11-26
    There are disclosed certain novel compounds identified as spiro piperidines and homologs which promote the release of growth hormone in humans and animals. This property can be utilized to promote the growth of food animals to render the production of edible meat products more efficient, and in humans, to treat physiological or medical conditions characterized by a deficiency in growth hormone secretion, such as short stature in growth hormone deficient children, and to treat medical conditions which are improved by the anabolic effects of growth hormone. Growth hormone releasing compositions containing such spiro compounds as the active ingredient thereof are also disclosed.
    已披露某些新型化合物,被确定为螺环哌啶和同系物,可以促进人类和动物体内生长激素的释放。这种特性可以用于促进食用动物的生长,使可食用肉制品的生产更加高效,在人类中,可用于治疗生长激素分泌不足所导致的生理或医学状况,如生长激素缺乏儿童的矮小身材,并用于治疗通过生长激素的合成效应得到改善的医学状况。还披露了含有这种螺环化合物作为活性成分的促生长激素组合物。
  • 6-(4-Hydroxy-phenyl)-3-alkyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
    申请人:SANOFI
    公开号:US20130085128A1
    公开(公告)日:2013-04-04
    The present invention relates to pyrazolo[3,4-b]pyridine compounds of the formula I, in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are defined as indicated below. The compounds of the formula I are kinase inhibitors, and are useful for the treatment of diseases associated with diabetes and diabetic complications, such as, diabetic nephropathy, diabetic neuropathy and diabetic retinopathy, for example. The invention furthermore relates to the use of compounds of the formula I, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.
    本发明涉及式I的吡唑并[3,4-b]吡啶化合物,其中R1、R2、R3、R4、R5、R6和R7如下所示。式I的化合物是激酶抑制剂,适用于治疗与糖尿病及糖尿病并发症相关的疾病,如糖尿病肾病、糖尿病神经病变和糖尿病视网膜病变等。此外,本发明还涉及式I的化合物的用途,特别是作为药物中的活性成分以及包含它们的药物组合物。
  • Amino-tetrazole analogues and methods of use
    申请人:Carroll A. William
    公开号:US20060052374A1
    公开(公告)日:2006-03-09
    A compound having Formula (I) or Formula (II) is disclosed as an P2X 7 antagonist, wherein A, B, C, Y, Y, Z, m, v, R 1 , R 2 , R 3 , R 4 , and R 5 , are as defined in the description. Methods and compositions for treating disease or condition modulated by P2X 7 are also disclosed.
    本文披露一种化合物,其化学式为(I)或(II),作为P2X7拮抗剂,其中A、B、C、Y、Y、Z、m、v、R1、R2、R3、R4和R5如描述中所定义。同时,本文还披露了治疗P2X7调节的疾病或病症的方法和组合物。
  • Amino-Tetrazoles Analogues and Methods of Use
    申请人:Carroll William A.
    公开号:US20080171733A1
    公开(公告)日:2008-07-17
    A compound having Formula (I) or Formula (II) is disclosed as an P2X 7 antagonist, wherein A, B, C, Y, Y, Z, m, v, R 1 , R 2 , R 3 , R 4 , and R 5 , are as defined in the description. Methods and compositions for treating disease or condition modulated by P2X 7 are also disclosed.
    本发明揭示了一种具有公式(I)或公式(II)的化合物,作为P2X7拮抗剂,其中A,B,C,Y,Y,Z,m,v,R1,R2,R3,R4和R5如描述中所定义。还揭示了用于治疗受P2X7调节的疾病或病况的方法和组合物。
  • Amino-tetrazoles analogues and methods of use
    申请人:Carroll A. William
    公开号:US20070049584A1
    公开(公告)日:2007-03-01
    A compound having Formula (I) or Formula (II) is disclosed as an P2X 7 antagonist, wherein A, B, C, Y, Y, Z, m, v, R 1 , R 2 , R 3 , R 4 , and R 5 , are as defined in the description. Methods and compositions for treating disease or condition modulated by P2X 7 are also disclosed.
    公开了一种化合物,其化学式为(I)或化学式(II),作为P2X7拮抗剂,其中A,B,C,Y,Y,Z,m,v,R1,R2,R3,R4和R5如说明中所定义。还公开了治疗受P2X7调节的疾病或病状的方法和组合物。
查看更多

同类化合物

(S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (R)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (4S,5R)-3,3a,8,8a-四氢茚并[1,2-d]-1,2,3-氧杂噻唑-2,2-二氧化物-3-羧酸叔丁酯 (3aS,8aR)-2-(吡啶-2-基)-8,8a-二氢-3aH-茚并[1,2-d]恶唑 (3aS,3''aS,8aR,8''aR)-2,2''-环戊二烯双[3a,8a-二氢-8H-茚并[1,2-d]恶唑] (1α,1'R,4β)-4-甲氧基-5''-甲基-6'-[5-(1-丙炔基-1)-3-吡啶基]双螺[环己烷-1,2'-[2H]indene 齐洛那平 鼠完 麝香 风铃醇 颜料黄138 雷美替胺杂质14 雷美替胺杂质 雷美替胺杂质 雷美替胺杂质 雷美替胺杂质 雷美替胺杂质 雷美替胺 雷沙吉兰杂质8 雷沙吉兰杂质5 雷沙吉兰杂质4 雷沙吉兰杂质3 雷沙吉兰杂质15 雷沙吉兰杂质12 雷沙吉兰杂质 雷沙吉兰 阿替美唑盐酸盐 铵2-(1,3-二氧代-2,3-二氢-1H-茚-2-基)-8-甲基-6-喹啉磺酸酯 金粉蕨辛 金粉蕨亭 重氮正癸烷 酸性黄3[CI47005] 酒石酸雷沙吉兰 还原茚三酮(二水) 还原茚三酮 过氧化,2,3-二氢-1H-茚-1-基1,1-二甲基乙基 表蕨素L 螺双茚满 螺[茚-2,4-哌啶]-1(3H)-酮盐酸盐 螺[茚-2,4'-哌啶]-1(3H)-酮 螺[茚-1,4-哌啶]-3(2H)-酮盐酸盐 螺[环丙烷-1,2'-茚满]-1'-酮 螺[二氢化茚-1,4'-哌啶] 螺[1H-茚-1,4-哌啶]-3(2H)-酮 螺[1H-茚-1,4-哌啶]-1,3-二羧酸, 2,3-二氢- 1,1-二甲基乙酯 螺[1,2-二氢茚-3,1'-环丙烷] 藏花茚 蕨素 Z 蕨素 D 蕨素 C