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(S)-9-{2-cyclopropyl-2-[(E)-methoxyimino]ethyl}-2-((R)-3-methylmorpholin-4-yl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one | 1523411-06-4

中文名称
——
中文别名
——
英文名称
(S)-9-{2-cyclopropyl-2-[(E)-methoxyimino]ethyl}-2-((R)-3-methylmorpholin-4-yl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one
英文别名
(8S)-9-[(2E)-2-cyclopropyl-2-methoxyiminoethyl]-2-[(3R)-3-methylmorpholin-4-yl]-8-(trifluoromethyl)-7,8-dihydro-6H-pyrimido[1,2-a]pyrimidin-4-one
(S)-9-{2-cyclopropyl-2-[(E)-methoxyimino]ethyl}-2-((R)-3-methylmorpholin-4-yl)-8-trifluoromethyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one化学式
CAS
1523411-06-4
化学式
C19H26F3N5O3
mdl
——
分子量
429.442
InChiKey
VBFOUPSVTKVNHJ-SWZXHNBJSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    30
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    70
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

点击查看最新优质反应信息

文献信息

  • Novel 2,3-Dihydro-1H-imidazopyrimidin-5-one and this 1,2,3,4-tetrahydropyrimidopyrimidin-6-one Derivatives Comprising a Substituted Morpholine, Preparation Thereof and Pharmaceutical Use Thereof
    申请人:SANOFI
    公开号:US20150148328A1
    公开(公告)日:2015-05-28
    The invention relates to the novel products of formula (I) with p, q=0, 1 or 2; R1=phenyl, pyridyl; —(CH 2 ) m —Ra; alkylene; cycloalkyl; heterocycloalkyl; alkyl; —SO 2 —Rb; —CO—Re; m=1 or 2; Ra=aryl, heteroaryl, —CO-cycloalkyl, —CO-heterocycloalkyl, —CO—Rb, —C(Rb)═N—ORc, —CO 2 Rd, —CONRxRy; Rb=alkyl, aryl, heteroaryl; Rc=H, alkyl; Rd=alkyl, cycloalkyl; Re=alkyl, cycloalkyl, aryl, heteroaryl; NRxRy with Rx,Ry=H, alkyl, cycloalkyl, alkoxy, phenyl, or form with N a ring with optionally O, N; R2, R3=H, alkyl, CF 3, or form with C a ring with optionally O, S and N; R4=H, F, Cl, CH 3 or CN; the morpholine is substituted with Me, and optionally substituted with F, OH; or is (Formula 1a) and the isomer of configuration R,R (Formula 1b) these products being in all the isomer forms and the salts, as medicaments, in particular as anticancer medicaments.
    本发明涉及公式(I)的新型产物,其中p,q = 0、1或2;R1 = 苯基、吡啶基;—(CH2)m—Ra;烷基;环烷基;杂环烷基;烷基;—SO2—Rb;—CO—Re;m = 1或2;Ra = 芳基、杂芳基、—CO-环烷基、—CO-杂环烷基、—CO—Rb、—C(Rb)═N—ORc、—CO2Rd、—CONRxRy;Rb = 烷基、芳基、杂芳基;Rc = H、烷基;Rd = 烷基、环烷基;Re = 烷基、环烷基、芳基、杂芳基;NRxRy,其中Rx,Ry = H、烷基、环烷基、烷氧基、苯基,或与N形成一个环,该环可以选择性地含有O、N;R2,R3 = H、烷基、CF3,或与C形成一个环,该环可以选择性地含有O、S和N;R4 = H、F、Cl、CH3或CN;吗啡环以Me取代,或以F、OH取代;或为(公式1a),具有R,R构型的异构体(公式1b)。这些产物以所有的异构体形式和盐形式作为药物,特别是作为抗癌药物。
  • 2,3-dihydro-1H-imidazo{1,2-a}pyrimidin-5-one and this 1,2,3,4-tetrahydropyrimido{1,2-a}pyrimidin-6-one derivatives comprising a substituted morpholine, preparation thereof and pharmaceutical use thereof
    申请人:SANOFI
    公开号:US10253043B2
    公开(公告)日:2019-04-09
    The invention relates to the novel products of formula (I) with p, q=0, 1 or 2; R1=phenyl, pyridyl; —(CH2)m—Ra; alkylene; cycloalkyl; heterocycloalkyl; alkyl; —SO2 —Rb; —CO—Re; m=1 or 2; Ra=aryl, heteroaryl, —CO-cycloalkyl, —CO-heterocycloalkyl, —CO—Rb, —C(Rb)═N—ORc, —CO 2 Rd, —CONRxRy; Rb=alkyl, aryl, heteroaryl; Rc=H, alkyl; Rd=alkyl, cycloalkyl; Re=alkyl, cycloalkyl, aryl, heteroaryl; NRxRy with Rx,Ry=H, alkyl, cycloalkyl, alkoxy, phenyl, or form with N a ring with optionally O, N; R2, R3=H, alkyl, CF 3, or form with C a ring with optionally O, S and N; R4=H, F, Cl, CH3 or CN; the morpholine is substituted with Me, and optionally substituted with F, OH; or is (Formula 1a) and the isomer of configuration R,R (Formula 1b) these products being in all the isomer forms and the salts, as medicaments, in particular as anticancer medicaments.
    本发明涉及式(I)的新型产品,其中 p、q=0、1 或 2;R1=苯基、吡啶基;-(CH2)m-Ra;亚烷基;环烷基;杂环烷基;烷基;-SO2 -Rb;-CO-Re;m=1 或 2;Ra=芳基、杂芳基、-CO-环烷基、-CO-杂环烷基、-CO-Rb、-C(Rb)═N-ORC、-CO 2 Rd、-CONRxRy;Rb=烷基、芳基、杂芳基;Rc=H、烷基;Rd=烷基、环烷基;Re=烷基、环烷基、芳基、杂芳基;NRxRy,其中 Rx、Ry=H、烷基、环烷基、烷氧基、苯基,或与 N 形成可选 O、N 的环;R2、R3=H、烷基、CF 3,或与 C 形成可选 O、S 和 N 的环;R4=H、F、Cl、CH3 或 CN;吗啉被 Me 取代,并可选被 F、OH 取代;或者是(式 1a)和构型为 R,R 的异构体(式 1b),这些产品以所有异构体形式和盐类作为药物,特别是抗癌药物。
  • Novel 2,3-Dihydro-1h-imidazo{1,2-a}pyrimidin-5-one and this 1,2,3,4-tetrahydropyrimido{1,2-a}pyrimidin-6-one Derivatives Comprising a Substituted Morpholine, Preparation Thereof and Pharmaceutical Use Thereof
    申请人:SANOFI
    公开号:US20190292205A1
    公开(公告)日:2019-09-26
    The invention relates to the novel products of formula (I): with p, q=0, 1 or 2; R1=phenyl, pyridyl; —(CH 2 ) m —Ra; alkylene; cycloalkyl; heterocycloalkyl; alkyl; —SO 2 —Rb; —CO—Re; m=1 or 2; Ra=aryl, heteroaryl, —CO-cycloalkyl, —CO-heterocycloalkyl, —CO—Rb, —C(Rb)═N—ORc, —CO 2 Rd, —CONRxRy; Rb=alkyl, aryl, heteroaryl; Rc=H, alkyl; Rd=alkyl, cycloalkyl; Re=alkyl, cycloalkyl, aryl, heteroaryl; NRxRy with Rx,Ry=H, alkyl, cycloalkyl, alkoxy, phenyl, or form with N a ring with optionally O, N; R2, R3=H, alkyl, CF 3 , or form with C a ring with optionally O, S and N; R4=H, F, Cl, CH 3 or CN; the morpholine is substituted with Me, and optionally substituted with F, OH; or is and the isomer of configuration R,R these products being in all the isomer forms and the salts, as medicaments, in particular as anticancer medicaments.
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