JP4156035B2 - ２−（プリン−９−イル）−テトラヒドロフラン−３，４−ジオール誘導体 - Google Patents

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Publication number

JP4156035B2

JP4156035B2 JP52838098A JP52838098A JP4156035B2 JP 4156035 B2 JP4156035 B2 JP 4156035B2 JP 52838098 A JP52838098 A JP 52838098A JP 52838098 A JP52838098 A JP 52838098A JP 4156035 B2 JP4156035 B2 JP 4156035B2

Authority

JP

Japan

Prior art keywords

tetrahydro

furan

ethylamino

diol

purin

Prior art date

1996-12-24

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired - Fee Related

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• YQUJSBYIKMQCIT-UHFFFAOYSA-N 2-purin-9-yloxolane-3,4-diol Chemical class OC1C(O)COC1N1C2=NC=NC=C2N=C1 YQUJSBYIKMQCIT-UHFFFAOYSA-N 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims description 269
• -1 tetrahydropyran-4-yl Chemical group 0.000 claims description 218
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 215
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 106
• 229910052757 nitrogen Inorganic materials 0.000 claims description 54
• 125000000217 alkyl group Chemical group 0.000 claims description 52
• 125000003118 aryl group Chemical group 0.000 claims description 49
• 238000000034 method Methods 0.000 claims description 33
• 150000003839 salts Chemical class 0.000 claims description 31
• 239000001257 hydrogen Substances 0.000 claims description 22
• 229910052739 hydrogen Inorganic materials 0.000 claims description 22
• 229910052736 halogen Inorganic materials 0.000 claims description 21
• 150000002367 halogens Chemical class 0.000 claims description 21
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 19
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 16
• 125000002252 acyl group Chemical group 0.000 claims description 15
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
• 230000008569 process Effects 0.000 claims description 15
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 14
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
• 239000012453 solvate Substances 0.000 claims description 14
• 239000011737 fluorine Substances 0.000 claims description 13
• 229910052731 fluorine Inorganic materials 0.000 claims description 13
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 12
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
• 239000000460 chlorine Substances 0.000 claims description 12
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
• BGRKDLVBPMCBJW-UHFFFAOYSA-N 2-ethyltetrazole Chemical compound CCN1N=CN=N1 BGRKDLVBPMCBJW-UHFFFAOYSA-N 0.000 claims description 10
• 150000002431 hydrogen Chemical class 0.000 claims description 10
• 150000001241 acetals Chemical class 0.000 claims description 9
• 208000027866 inflammatory disease Diseases 0.000 claims description 9
• 239000008194 pharmaceutical composition Substances 0.000 claims description 9
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
• 229910052801 chlorine Inorganic materials 0.000 claims description 8
• 125000004911 3,3-dimethylbutylamino group Chemical group CC(CCN*)(C)C 0.000 claims description 6
• 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
• 238000002360 preparation method Methods 0.000 claims description 6
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 6
• VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
• 208000006673 asthma Diseases 0.000 claims description 5
• 125000002785 azepinyl group Chemical group 0.000 claims description 5
• 125000002393 azetidinyl group Chemical group 0.000 claims description 5
• 150000002148 esters Chemical group 0.000 claims description 5
• VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
• 125000002757 morpholinyl group Chemical group 0.000 claims description 5
• 229910052760 oxygen Inorganic materials 0.000 claims description 5
• 125000004193 piperazinyl group Chemical group 0.000 claims description 5
• 125000003386 piperidinyl group Chemical group 0.000 claims description 5
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 5
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 5
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
• 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 4
• 125000003545 alkoxy group Chemical group 0.000 claims description 4
• SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical group C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 claims description 4
• 229910052717 sulfur Inorganic materials 0.000 claims description 4
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
• 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 3
• 239000003085 diluting agent Substances 0.000 claims description 3
• 229910052740 iodine Inorganic materials 0.000 claims description 3
• 125000005322 morpholin-1-yl group Chemical group 0.000 claims description 3
• 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims description 3
• 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims description 3
• 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 3
• SWJQFNZODOMOSK-CMCWBKRRSA-N (2r,3r,4s,5r)-2-[6-(benzylamino)-2-[2-(1-methylimidazol-4-yl)ethylamino]purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=CN(C)C=4)=NC(NCC=4C=CC=CC=4)=C3N=C2)O)=N1 SWJQFNZODOMOSK-CMCWBKRRSA-N 0.000 claims description 2
• PBAHFWUQEPDDAU-CMCWBKRRSA-N (2r,3s,4r,5r)-2-(2-ethyltetrazol-5-yl)-5-[6-[(3-iodophenyl)methylamino]-2-[2-(1-methylimidazol-4-yl)ethylamino]purin-9-yl]oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=CN(C)C=4)=NC(NCC=4C=C(I)C=CC=4)=C3N=C2)O)=N1 PBAHFWUQEPDDAU-CMCWBKRRSA-N 0.000 claims description 2
• VRESBNUEIKZECD-UHFFFAOYSA-N 2-methyltetrazole Chemical compound CN1N=CN=N1 VRESBNUEIKZECD-UHFFFAOYSA-N 0.000 claims description 2
• 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 2
• XQEZVPLQUSABJR-UZKMKHCNSA-N CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(N[C@@H]4CC[C@@H](N)CC4)=NC(N)=C3N=C2)O)=N1 Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(N[C@@H]4CC[C@@H](N)CC4)=NC(N)=C3N=C2)O)=N1 XQEZVPLQUSABJR-UZKMKHCNSA-N 0.000 claims description 2
• 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
• 125000004432 carbon atom Chemical group C* 0.000 claims description 2
• 239000000969 carrier Substances 0.000 claims description 2
• RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 2
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
• DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 8
• GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims 5
• 101150065749 Churc1 gene Proteins 0.000 claims 5
• 102100038239 Protein Churchill Human genes 0.000 claims 5
• 125000003277 amino group Chemical group 0.000 claims 5
• GUCHKXYEXZMOHO-UHFFFAOYSA-N 2-propan-2-yltetrazole Chemical compound CC(C)N1N=CN=N1 GUCHKXYEXZMOHO-UHFFFAOYSA-N 0.000 claims 2
• IYKRXRDKKGWFJC-XJSPFCSUSA-N (2R,3R,4S,5R)-2-[6-(2,2-diphenylethylamino)-2-[[(1R,2R)-2-hydroxycyclopentyl]amino]purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound C1(=CC=CC=C1)C(CNC1=C2N=CN(C2=NC(=N1)N[C@H]1[C@@H](CCC1)O)[C@@H]1O[C@@H]([C@H]([C@H]1O)O)C=1N=NN(N=1)C)C1=CC=CC=C1 IYKRXRDKKGWFJC-XJSPFCSUSA-N 0.000 claims 1
• RMMGOQSXDVKYOS-BUIUIBKASA-N (2R,3R,4S,5R)-2-[6-(3,3-dimethylbutylamino)-2-[[(1R,2R)-2-hydroxycyclopentyl]amino]purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CC(CCNC1=C2N=CN(C2=NC(=N1)N[C@H]1[C@@H](CCC1)O)[C@@H]1O[C@@H]([C@H]([C@H]1O)O)C=1N=NN(N=1)CC)(C)C RMMGOQSXDVKYOS-BUIUIBKASA-N 0.000 claims 1
• JSKQVJFMOAQHOD-QPXQOZNCSA-N (2r,3r,4s,5r)-2-[2-(2-morpholin-4-ylethylamino)-6-(pentan-3-ylamino)purin-9-yl]-5-(2-propan-2-yltetrazol-5-yl)oxolane-3,4-diol Chemical compound N=1C=2N([C@H]3[C@@H]([C@H](O)[C@H](O3)C3=NN(N=N3)C(C)C)O)C=NC=2C(NC(CC)CC)=NC=1NCCN1CCOCC1 JSKQVJFMOAQHOD-QPXQOZNCSA-N 0.000 claims 1
• CDXIYBLQSCIRLM-GGRAJKFRSA-N (2r,3r,4s,5r)-2-[2-[(1-benzylpyrrolidin-3-yl)amino]-6-(2-phenylethylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NC4CN(CC=5C=CC=CC=5)CC4)=NC(NCCC=4C=CC=CC=4)=C3N=C2)O)=N1 CDXIYBLQSCIRLM-GGRAJKFRSA-N 0.000 claims 1
• QFHBJRRQXVLZDI-OSKDKKHNSA-N (2r,3r,4s,5r)-2-[2-[(1-benzylpyrrolidin-3-yl)amino]-6-(pentan-3-ylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound N=1C=2N([C@H]3[C@@H]([C@H](O)[C@H](O3)C3=NN(CC)N=N3)O)C=NC=2C(NC(CC)CC)=NC=1NC(C1)CCN1CC1=CC=CC=C1 QFHBJRRQXVLZDI-OSKDKKHNSA-N 0.000 claims 1
• SPWDITYEUXYDIE-SLWWVJOCSA-N (2r,3r,4s,5r)-2-[2-[(1-benzylpyrrolidin-3-yl)amino]-6-[(3-iodophenyl)methylamino]purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NC4CN(CC=5C=CC=CC=5)CC4)=NC(NCC=4C=C(I)C=CC=4)=C3N=C2)O)=N1 SPWDITYEUXYDIE-SLWWVJOCSA-N 0.000 claims 1
• XOLLYEDWBOGTPT-IMIIHFCZSA-N (2r,3r,4s,5r)-2-[2-[2-(1-methylimidazol-4-yl)ethylamino]-6-(2-phenylethylamino)purin-9-yl]-5-(2-propan-2-yltetrazol-5-yl)oxolane-3,4-diol Chemical compound CC(C)N1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=CN(C)C=4)=NC(NCCC=4C=CC=CC=4)=C3N=C2)O)=N1 XOLLYEDWBOGTPT-IMIIHFCZSA-N 0.000 claims 1
• USVQYAKJZJPSRK-GRXQJBFDSA-N (2r,3r,4s,5r)-2-[2-[2-(1-methylimidazol-4-yl)ethylamino]-6-(pentan-3-ylamino)purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound N=1C=2N([C@H]3[C@@H]([C@H](O)[C@H](O3)C3=NN(C)N=N3)O)C=NC=2C(NC(CC)CC)=NC=1NCCC1=CN(C)C=N1 USVQYAKJZJPSRK-GRXQJBFDSA-N 0.000 claims 1
• ISCXSHUNHLUVST-QPXQOZNCSA-N (2r,3r,4s,5r)-2-[2-[2-(1-methylimidazol-4-yl)ethylamino]-6-(pentan-3-ylamino)purin-9-yl]-5-(2-propan-2-yltetrazol-5-yl)oxolane-3,4-diol Chemical compound N=1C=2N([C@H]3[C@@H]([C@H](O)[C@H](O3)C3=NN(N=N3)C(C)C)O)C=NC=2C(NC(CC)CC)=NC=1NCCC1=CN(C)C=N1 ISCXSHUNHLUVST-QPXQOZNCSA-N 0.000 claims 1
• HOXQRVLGKMUTKR-CKXMCULTSA-N (2r,3r,4s,5r)-2-[2-[2-(6-aminopyridin-2-yl)ethylamino]-6-(2,2-diphenylethylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=C(N)C=CC=4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 HOXQRVLGKMUTKR-CKXMCULTSA-N 0.000 claims 1
• CCYUSUQOSHABQD-OVDFTCDZSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-morpholin-4-ylethylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCN4CCOCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 CCYUSUQOSHABQD-OVDFTCDZSA-N 0.000 claims 1
• AEMTVBKNDCUVDN-YRIIQKNPSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-morpholin-4-ylethylamino)purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCN4CCOCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 AEMTVBKNDCUVDN-YRIIQKNPSA-N 0.000 claims 1
• VIFOOODREXJSEK-CKXMCULTSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-piperidin-1-ylethylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCN4CCCCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 VIFOOODREXJSEK-CKXMCULTSA-N 0.000 claims 1
• RTXZDJRVDCPRJU-OVDFTCDZSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-piperidin-1-ylethylamino)purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCN4CCCCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 RTXZDJRVDCPRJU-OVDFTCDZSA-N 0.000 claims 1
• MCAUZAFWRKMFHY-OVDFTCDZSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-pyridin-2-ylethylamino)purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=CC=CC=4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 MCAUZAFWRKMFHY-OVDFTCDZSA-N 0.000 claims 1
• RLUQLDFOCWLMSH-OVDFTCDZSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(2-pyrrolidin-1-ylethylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCN4CCCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 RLUQLDFOCWLMSH-OVDFTCDZSA-N 0.000 claims 1
• RTJYHJSEKLXQPL-YRIIQKNPSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(oxan-4-ylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NC4CCOCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 RTJYHJSEKLXQPL-YRIIQKNPSA-N 0.000 claims 1
• NTGVVIJCALQADM-MMSSMPOCSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(pyrrolidin-3-ylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NC4CNCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 NTGVVIJCALQADM-MMSSMPOCSA-N 0.000 claims 1
• RMVMOEOKCYTKAQ-YRIIQKNPSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-(thian-4-ylamino)purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NC4CCSCC4)=NC(NCC(C=4C=CC=CC=4)C=4C=CC=CC=4)=C3N=C2)O)=N1 RMVMOEOKCYTKAQ-YRIIQKNPSA-N 0.000 claims 1
• RFZYXTIQPZEWFB-YRIIQKNPSA-N (2r,3r,4s,5r)-2-[6-(2,2-diphenylethylamino)-2-[2-(1-methylimidazol-4-yl)ethylamino]purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CN1C=NC(CCNC=2N=C3N([C@H]4[C@@H]([C@H](O)[C@H](O4)C4=NN(C)N=N4)O)C=NC3=C(NCC(C=3C=CC=CC=3)C=3C=CC=CC=3)N=2)=C1 RFZYXTIQPZEWFB-YRIIQKNPSA-N 0.000 claims 1
• RPTLPICWRONXMP-CMCWBKRRSA-N (2r,3r,4s,5r)-2-[6-(2-cyclohexylethylamino)-2-[2-(1-methylimidazol-4-yl)ethylamino]purin-9-yl]-5-(2-methyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CN1C=NC(CCNC=2N=C3N([C@H]4[C@@H]([C@H](O)[C@H](O4)C4=NN(C)N=N4)O)C=NC3=C(NCCC3CCCCC3)N=2)=C1 RPTLPICWRONXMP-CMCWBKRRSA-N 0.000 claims 1
• CMJVPOARTDAFBV-RQXXJAGISA-N (2r,3r,4s,5r)-2-[6-(3,3-dimethylbutylamino)-2-[2-(1-methylimidazol-4-yl)ethylamino]purin-9-yl]-5-(2-ethyltetrazol-5-yl)oxolane-3,4-diol Chemical compound CCN1N=NC([C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC(NCCC=4N=CN(C)C=4)=NC(NCCC(C)(C)C)=C3N=C2)O)=N1 CMJVPOARTDAFBV-RQXXJAGISA-N 0.000 claims 1
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