WO2009069100A1 - Phosphonic acid derivates and their use as p2y12 receptor antagonists - Google Patents
Phosphonic acid derivates and their use as p2y12 receptor antagonists Download PDFInfo
- Publication number
- WO2009069100A1 WO2009069100A1 PCT/IB2008/055002 IB2008055002W WO2009069100A1 WO 2009069100 A1 WO2009069100 A1 WO 2009069100A1 IB 2008055002 W IB2008055002 W IB 2008055002W WO 2009069100 A1 WO2009069100 A1 WO 2009069100A1
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- WO
- WIPO (PCT)
- Prior art keywords
- phenyl
- carbonyl
- pyrimidine
- amino
- piperazine
- Prior art date
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- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 title abstract description 10
- 229940127424 P2Y12 Receptor Antagonists Drugs 0.000 title abstract description 3
- 238000011282 treatment Methods 0.000 claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims description 577
- -1 hydroxy, hydroxymethyl Chemical group 0.000 claims description 158
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 claims description 153
- 150000003839 salts Chemical class 0.000 claims description 143
- 125000000217 alkyl group Chemical group 0.000 claims description 110
- 229910052757 nitrogen Inorganic materials 0.000 claims description 91
- 125000000623 heterocyclic group Chemical group 0.000 claims description 70
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 65
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 64
- 239000001257 hydrogen Substances 0.000 claims description 61
- 229910052739 hydrogen Inorganic materials 0.000 claims description 61
- 125000003545 alkoxy group Chemical group 0.000 claims description 53
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 49
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 47
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 29
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 28
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 23
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 125000004849 alkoxymethyl group Chemical group 0.000 claims description 18
- 239000003814 drug Substances 0.000 claims description 18
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 15
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims description 14
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 14
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
- 125000002883 imidazolyl group Chemical group 0.000 claims description 9
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 9
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 9
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims description 7
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims description 7
- XSEQYYOXBPJMIR-IGKIAQTJSA-N [4-[(2s)-3-(4-ethoxycarbonylpiperazin-1-yl)-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CC1=CC=C(P(O)(O)=O)C=C1 XSEQYYOXBPJMIR-IGKIAQTJSA-N 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- ZXJZEJVFJBBIRW-FQEVSTJZSA-N [(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-(2-hydroxyethoxy)-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(OCCO)=NC(C=2C=CC=CC=2)=N1 ZXJZEJVFJBBIRW-FQEVSTJZSA-N 0.000 claims description 4
- YTAUPEZWFNCNBZ-CTLOQAHHSA-N [2-[2-(4-butoxycarbonylpiperazin-1-yl)-1-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-2-oxoethyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)C(C=1C(=CC=CC=1)P(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 YTAUPEZWFNCNBZ-CTLOQAHHSA-N 0.000 claims description 4
- GNCLYDRJKVFSPD-GMMLNUAGSA-N [3-[2-(4-butoxycarbonylpiperazin-1-yl)-1-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-2-oxoethyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)C(C=1C=C(C=CC=1)P(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 GNCLYDRJKVFSPD-GMMLNUAGSA-N 0.000 claims description 4
- KUFSGJUDTJTJJX-DCCUJTHKSA-N [3-[2-(4-ethoxycarbonylpiperazin-1-yl)-1-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-2-oxoethyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCC)CCN1C(=O)C(C=1C=C(C=CC=1)P(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 KUFSGJUDTJTJJX-DCCUJTHKSA-N 0.000 claims description 4
- IPPVDPLZYBRZDT-JDXGNMNLSA-N [4-[(2s)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phenyl]methylphosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CC1=CC=C(CP(O)(O)=O)C=C1 IPPVDPLZYBRZDT-JDXGNMNLSA-N 0.000 claims description 4
- BYVKMTXSIMUWIF-WNJJXGMVSA-N [4-[(2s)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CC1=CC=C(P(O)(O)=O)C=C1 BYVKMTXSIMUWIF-WNJJXGMVSA-N 0.000 claims description 4
- HFOYTSRCWYVJQB-XCZPVHLTSA-N [4-[(2s)-3-(4-ethoxycarbonylpiperazin-1-yl)-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phenyl]methylphosphonic acid Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CC1=CC=C(CP(O)(O)=O)C=C1 HFOYTSRCWYVJQB-XCZPVHLTSA-N 0.000 claims description 4
- JXUBCDKYFUXBIZ-GMMLNUAGSA-N [4-[2-(4-butoxycarbonylpiperazin-1-yl)-1-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-2-oxoethyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)C(C=1C=CC(=CC=1)P(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 JXUBCDKYFUXBIZ-GMMLNUAGSA-N 0.000 claims description 4
- MMRJFTURRVEHMQ-DCCUJTHKSA-N [4-[2-(4-ethoxycarbonylpiperazin-1-yl)-1-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-2-oxoethyl]phenyl]phosphonic acid Chemical compound C1CN(C(=O)OCC)CCN1C(=O)C(C=1C=CC(=CC=1)P(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 MMRJFTURRVEHMQ-DCCUJTHKSA-N 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 125000004494 ethyl ester group Chemical group 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 208000019553 vascular disease Diseases 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- IGTVOTZFNVCPIU-YTMVLYRLSA-N [(2R)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3S)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropylidene]-[di(butanoyloxy)methoxy]-oxidophosphanium Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](C=P(=O)OC(OC(=O)CCC)OC(=O)CCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 IGTVOTZFNVCPIU-YTMVLYRLSA-N 0.000 claims description 3
- SKPOMRGCFYKOJR-BDYUSTAISA-N [(2R)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3S)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropylidene]-[di(propanoyloxy)methoxy]-oxidophosphanium Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](C=P(=O)OC(OC(=O)CC)OC(=O)CC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 SKPOMRGCFYKOJR-BDYUSTAISA-N 0.000 claims description 3
- KYYQEBSLEMOPEO-QFIPXVFZSA-N [(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[(6-morpholin-4-yl-2-phenylpyrimidine-4-carbonyl)amino]-3-oxopropyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(N2CCOCC2)=NC(C=2C=CC=CC=2)=N1 KYYQEBSLEMOPEO-QFIPXVFZSA-N 0.000 claims description 3
- ZJTCYSPTLFEVPH-QHCPKHFHSA-N [(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-(4-methylpiperazin-1-yl)-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(N2CCN(C)CC2)=NC(C=2C=CC=CC=2)=N1 ZJTCYSPTLFEVPH-QHCPKHFHSA-N 0.000 claims description 3
- LNTMATIVLLGIGK-QHCPKHFHSA-N [(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[3-(methoxymethyl)azetidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(N2CC(COC)C2)=NC(C=2C=CC=CC=2)=N1 LNTMATIVLLGIGK-QHCPKHFHSA-N 0.000 claims description 3
- WQCWUBJLTUBDLU-QFIPXVFZSA-N [(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-3-oxo-2-[(2-phenyl-6-propan-2-ylpyrimidine-4-carbonyl)amino]propyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(C(C)C)=NC(C=2C=CC=CC=2)=N1 WQCWUBJLTUBDLU-QFIPXVFZSA-N 0.000 claims description 3
- JUQBEMMMBAKFBJ-BJKOFHAPSA-N [(4r)-5-(4-butoxycarbonylpiperazin-1-yl)-4-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-5-oxopentyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](CCCP(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 JUQBEMMMBAKFBJ-BJKOFHAPSA-N 0.000 claims description 3
- JUQBEMMMBAKFBJ-ZEQRLZLVSA-N [(4s)-5-(4-butoxycarbonylpiperazin-1-yl)-4-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-5-oxopentyl]phosphonic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CCCP(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 JUQBEMMMBAKFBJ-ZEQRLZLVSA-N 0.000 claims description 3
- MQAOVLHAVIBNAY-AHWVRZQESA-N acetyloxymethoxy-[(2r)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropyl]phosphinic acid Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(=O)OCOC(C)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 MQAOVLHAVIBNAY-AHWVRZQESA-N 0.000 claims description 3
- MNOYKEOAZCXQAU-PUUNBFJPSA-N butyl 4-[(2r)-3-[bis(1-ethoxycarbonyloxyethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(=O)(OC(C)OC(=O)OCC)OC(C)OC(=O)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 MNOYKEOAZCXQAU-PUUNBFJPSA-N 0.000 claims description 3
- DZWWOUXSLVZXAX-REKAVORPSA-N butyl 4-[(2r)-3-[bis(1-propan-2-yloxycarbonyloxyethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(=O)(OC(C)OC(=O)OC(C)C)OC(C)OC(=O)OC(C)C)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 DZWWOUXSLVZXAX-REKAVORPSA-N 0.000 claims description 3
- ODMDAAXOPRGRLA-YTMVLYRLSA-N butyl 4-[(2r)-3-[bis(acetyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(=O)(OCOC(C)=O)OCOC(C)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 ODMDAAXOPRGRLA-YTMVLYRLSA-N 0.000 claims description 3
- ZALLVONZQZIMCH-ILUGTUFDSA-N butyl 4-[(2r)-3-bis[[(2s)-1-ethoxy-1-oxopropan-2-yl]oxy]phosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(=O)(O[C@@H](C)C(=O)OCC)O[C@@H](C)C(=O)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 ZALLVONZQZIMCH-ILUGTUFDSA-N 0.000 claims description 3
- QSOZEHIASCYOEA-LRHLLKFHSA-N butyl 4-[(2r)-3-diphenoxyphosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 QSOZEHIASCYOEA-LRHLLKFHSA-N 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- BIICBLXOQXGKFB-BDYUSTAISA-N ethyl 4-[(2r)-3-[bis(acetyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@H](CP(=O)(OCOC(C)=O)OCOC(C)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 BIICBLXOQXGKFB-BDYUSTAISA-N 0.000 claims description 3
- BIICBLXOQXGKFB-AHKZPQOWSA-N ethyl 4-[(2s)-3-[bis(acetyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](CP(=O)(OCOC(C)=O)OCOC(C)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 BIICBLXOQXGKFB-AHKZPQOWSA-N 0.000 claims description 3
- NBIQFKPKGYYHGL-BDYUSTAISA-N [(2R)-3-(4-butoxycarbonylpiperazin-1-yl)-2-[[6-[(3S)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropylidene]-(1,3-diethoxy-1,3-dioxopropan-2-yl)oxy-oxidophosphanium Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](C=P(=O)OC(C(=O)OCC)C(=O)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 NBIQFKPKGYYHGL-BDYUSTAISA-N 0.000 claims description 2
- SNQPOAHBMGFJJT-NRFANRHFSA-N [(2r)-2-[(6-cyclopentyloxy-2-phenylpyrimidine-4-carbonyl)amino]-3-(4-ethoxycarbonylpiperazin-1-yl)-3-oxopropyl]phosphonic acid Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(OC2CCCC2)=NC(C=2C=CC=CC=2)=N1 SNQPOAHBMGFJJT-NRFANRHFSA-N 0.000 claims description 2
- KQUVGYMFBWPPQO-NPRSNXAQSA-N butyl 4-[(2r)-3-[bis(1-cyclohexyloxycarbonyloxyethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CP(=O)(OC(C)OC(=O)OC1CCCCC1)OC(C)OC(=O)OC1CCCCC1 KQUVGYMFBWPPQO-NPRSNXAQSA-N 0.000 claims description 2
- JYYKYKRSHVVVQT-JSXFGMRASA-N butyl 4-[(2r)-3-bis(phenylmethoxy)phosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CP(=O)(OCC=1C=CC=CC=1)OCC1=CC=CC=C1 JYYKYKRSHVVVQT-JSXFGMRASA-N 0.000 claims description 2
- AILAQOYFPLQIFN-UHFFFAOYSA-N butyl piperazine-1-carboxylate Chemical compound CCCCOC(=O)N1CCNCC1 AILAQOYFPLQIFN-UHFFFAOYSA-N 0.000 claims description 2
- PCUISYIUKKPEIH-BDYUSTAISA-N di(butanoyloxy)methoxy-[(2R)-3-(4-ethoxycarbonylpiperazin-1-yl)-2-[[6-[(3S)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropylidene]-oxidophosphanium Chemical compound N([C@@H](C=P(=O)OC(OC(=O)CCC)OC(=O)CCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 PCUISYIUKKPEIH-BDYUSTAISA-N 0.000 claims description 2
- PCUISYIUKKPEIH-AHKZPQOWSA-N di(butanoyloxy)methoxy-[(2S)-3-(4-ethoxycarbonylpiperazin-1-yl)-2-[[6-[(3S)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]-3-oxopropylidene]-oxidophosphanium Chemical compound N([C@H](C=P(=O)OC(OC(=O)CCC)OC(=O)CCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 PCUISYIUKKPEIH-AHKZPQOWSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 abstract description 11
- 208000007536 Thrombosis Diseases 0.000 abstract description 6
- 230000002265 prevention Effects 0.000 abstract description 5
- 230000002792 vascular Effects 0.000 abstract description 5
- 230000002526 effect on cardiovascular system Effects 0.000 abstract description 4
- 241000124008 Mammalia Species 0.000 abstract description 3
- 208000026106 cerebrovascular disease Diseases 0.000 abstract description 3
- 230000002093 peripheral effect Effects 0.000 abstract description 3
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical class C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 description 503
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 348
- 238000000034 method Methods 0.000 description 285
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 246
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 104
- YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Natural products ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 103
- 239000012071 phase Substances 0.000 description 99
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- SCPQIIUACZUJKX-VWLOTQADSA-N ethyl 4-[(2r)-2-[(6-cyclopentyloxy-2-phenylpyrimidine-4-carbonyl)amino]-3-diethoxyphosphorylpropanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@H](CP(=O)(OCC)OCC)NC(=O)C1=CC(OC2CCCC2)=NC(C=2C=CC=CC=2)=N1 SCPQIIUACZUJKX-VWLOTQADSA-N 0.000 description 1
- BCKZDWFSGKAPRR-ABLWVSNPSA-N ethyl 4-[(2r)-2-amino-3-diethoxyphosphorylpropanoyl]-2-methylpiperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@@H](N)CP(=O)(OCC)OCC)CC1C BCKZDWFSGKAPRR-ABLWVSNPSA-N 0.000 description 1
- WOHKFNSREBNOKJ-CYBMUJFWSA-N ethyl 4-[(2r)-2-amino-4-diethoxyphosphorylbutanoyl]piperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@H](N)CCP(=O)(OCC)OCC)CC1 WOHKFNSREBNOKJ-CYBMUJFWSA-N 0.000 description 1
- UNDPUUOUQURCRS-YTMVLYRLSA-N ethyl 4-[(2r)-3-[bis(butanoyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound N([C@@H](CP(=O)(OCOC(=O)CCC)OCOC(=O)CCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 UNDPUUOUQURCRS-YTMVLYRLSA-N 0.000 description 1
- BEQAJHHRSVGCHH-BDYUSTAISA-N ethyl 4-[(2r)-3-[bis(ethoxycarbonyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound N([C@@H](CP(=O)(OCOC(=O)OCC)OCOC(=O)OCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 BEQAJHHRSVGCHH-BDYUSTAISA-N 0.000 description 1
- HGEQOFUDZWHKGA-LYKKTTPLSA-N ethyl 4-[(2r)-3-diethoxyphosphoryl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]-2-methylpiperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@H](CP(=O)(OCC)OCC)NC(=O)OC(C)(C)C)CC1C HGEQOFUDZWHKGA-LYKKTTPLSA-N 0.000 description 1
- MVAMGUCIWYVFQR-HNNXBMFYSA-N ethyl 4-[(2r)-3-diethoxyphosphoryl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]piperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@H](CP(=O)(OCC)OCC)NC(=O)OC(C)(C)C)CC1 MVAMGUCIWYVFQR-HNNXBMFYSA-N 0.000 description 1
- KVYPZQHLNYBSHU-MMOCMJAISA-N ethyl 4-[(2r)-3-diethoxyphosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]-2-methylpiperazine-1-carboxylate Chemical compound C1C(C)N(C(=O)OCC)CCN1C(=O)[C@H](CP(=O)(OCC)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 KVYPZQHLNYBSHU-MMOCMJAISA-N 0.000 description 1
- JHZYIQWMQCIMDE-HXUWFJFHSA-N ethyl 4-[(2r)-4-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)butanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](CCP(=O)(OCC)OCC)NC(=O)OCC1=CC=CC=C1 JHZYIQWMQCIMDE-HXUWFJFHSA-N 0.000 description 1
- NGWLKIZQAHFOGQ-LOSJGSFVSA-N ethyl 4-[(2r)-4-diethoxyphosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]butanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](CCP(=O)(OCC)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 NGWLKIZQAHFOGQ-LOSJGSFVSA-N 0.000 description 1
- IXHZHCXVYHEVPB-FERBBOLQSA-N ethyl 4-[(2s)-2-amino-3-(3-diethoxyphosphorylphenyl)propanoyl]piperazine-1-carboxylate;hydrochloride Chemical compound Cl.C1CN(C(=O)OCC)CCN1C(=O)[C@@H](N)CC1=CC=CC(P(=O)(OCC)OCC)=C1 IXHZHCXVYHEVPB-FERBBOLQSA-N 0.000 description 1
- QEEONLJUYYDPRK-FERBBOLQSA-N ethyl 4-[(2s)-2-amino-3-(4-diethoxyphosphorylphenyl)propanoyl]piperazine-1-carboxylate;hydrochloride Chemical compound Cl.C1CN(C(=O)OCC)CCN1C(=O)[C@@H](N)CC1=CC=C(P(=O)(OCC)OCC)C=C1 QEEONLJUYYDPRK-FERBBOLQSA-N 0.000 description 1
- YHIAYNCPCSIXNR-IBGZPJMESA-N ethyl 4-[(2s)-2-amino-3-[4-(diethoxyphosphorylmethyl)phenyl]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](N)CC1=CC=C(CP(=O)(OCC)OCC)C=C1 YHIAYNCPCSIXNR-IBGZPJMESA-N 0.000 description 1
- LUXHSGPAYDJRGV-UTONKHPSSA-N ethyl 4-[(2s)-2-amino-3-diethoxyphosphorylpropanoyl]piperazine-1-carboxylate;hydrochloride Chemical compound Cl.CCOC(=O)N1CCN(C(=O)[C@H](N)CP(=O)(OCC)OCC)CC1 LUXHSGPAYDJRGV-UTONKHPSSA-N 0.000 description 1
- WOHKFNSREBNOKJ-ZDUSSCGKSA-N ethyl 4-[(2s)-2-amino-4-diethoxyphosphorylbutanoyl]piperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@@H](N)CCP(=O)(OCC)OCC)CC1 WOHKFNSREBNOKJ-ZDUSSCGKSA-N 0.000 description 1
- FTEPMPONEWMFPB-NRFANRHFSA-N ethyl 4-[(2s)-3-(3-diethoxyphosphorylphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](NC(=O)OC(C)(C)C)CC1=CC=CC(P(=O)(OCC)OCC)=C1 FTEPMPONEWMFPB-NRFANRHFSA-N 0.000 description 1
- UFLZUUCGPXTDHA-NRFANRHFSA-N ethyl 4-[(2s)-3-(4-diethoxyphosphorylphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](NC(=O)OC(C)(C)C)CC1=CC=C(P(=O)(OCC)OCC)C=C1 UFLZUUCGPXTDHA-NRFANRHFSA-N 0.000 description 1
- SEWOABDFJYQGQL-CDZUIXILSA-N ethyl 4-[(2s)-3-[4-(diethoxyphosphorylmethyl)phenyl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@@H](NC(=O)C=1N=C(N=C(C=1)N1C[C@H](CC1)OC)C=1C=CC=CC=1)CC1=CC=C(CP(=O)(OCC)OCC)C=C1 SEWOABDFJYQGQL-CDZUIXILSA-N 0.000 description 1
- LPLFKHBLJCDDHB-SHUZPENHSA-N ethyl 4-[(2s)-3-[4-[bis(butanoyloxymethoxy)phosphoryl]phenyl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1=CC(P(=O)(OCOC(=O)CCC)OCOC(=O)CCC)=CC=C1C[C@@H](C(=O)N1CCN(CC1)C(=O)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 LPLFKHBLJCDDHB-SHUZPENHSA-N 0.000 description 1
- RXRMMTXADRBIKJ-DITALETJSA-N ethyl 4-[(2s)-3-[4-[bis(ethoxycarbonyloxymethoxy)phosphoryl]phenyl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound C1=CC(P(=O)(OCOC(=O)OCC)OCOC(=O)OCC)=CC=C1C[C@@H](C(=O)N1CCN(CC1)C(=O)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 RXRMMTXADRBIKJ-DITALETJSA-N 0.000 description 1
- UNDPUUOUQURCRS-LMSSTIIKSA-N ethyl 4-[(2s)-3-[bis(butanoyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound N([C@H](CP(=O)(OCOC(=O)CCC)OCOC(=O)CCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 UNDPUUOUQURCRS-LMSSTIIKSA-N 0.000 description 1
- BEQAJHHRSVGCHH-AHKZPQOWSA-N ethyl 4-[(2s)-3-[bis(ethoxycarbonyloxymethoxy)phosphoryl]-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]propanoyl]piperazine-1-carboxylate Chemical compound N([C@H](CP(=O)(OCOC(=O)OCC)OCOC(=O)OCC)C(=O)N1CCN(CC1)C(=O)OCC)C(=O)C(N=1)=CC(N2C[C@H](CC2)OC)=NC=1C1=CC=CC=C1 BEQAJHHRSVGCHH-AHKZPQOWSA-N 0.000 description 1
- MVAMGUCIWYVFQR-OAHLLOKOSA-N ethyl 4-[(2s)-3-diethoxyphosphoryl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]piperazine-1-carboxylate Chemical compound CCOC(=O)N1CCN(C(=O)[C@@H](CP(=O)(OCC)OCC)NC(=O)OC(C)(C)C)CC1 MVAMGUCIWYVFQR-OAHLLOKOSA-N 0.000 description 1
- JHZYIQWMQCIMDE-FQEVSTJZSA-N ethyl 4-[(2s)-4-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)butanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@H](CCP(=O)(OCC)OCC)NC(=O)OCC1=CC=CC=C1 JHZYIQWMQCIMDE-FQEVSTJZSA-N 0.000 description 1
- NGWLKIZQAHFOGQ-DQEYMECFSA-N ethyl 4-[(2s)-4-diethoxyphosphoryl-2-[[6-[(3s)-3-methoxypyrrolidin-1-yl]-2-phenylpyrimidine-4-carbonyl]amino]butanoyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)[C@H](CCP(=O)(OCC)OCC)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 NGWLKIZQAHFOGQ-DQEYMECFSA-N 0.000 description 1
- COEMQNGVVXCMGH-UHFFFAOYSA-N ethyl 4-[2-(3-diethoxyphosphorylphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)C(NC(=O)OC(C)(C)C)C1=CC=CC(P(=O)(OCC)OCC)=C1 COEMQNGVVXCMGH-UHFFFAOYSA-N 0.000 description 1
- FKWRXTTYOFJRNI-UHFFFAOYSA-N ethyl 4-[2-(4-diethoxyphosphorylphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)C(NC(=O)OC(C)(C)C)C1=CC=C(P(=O)(OCC)OCC)C=C1 FKWRXTTYOFJRNI-UHFFFAOYSA-N 0.000 description 1
- UWELFCKWEVHBGN-UHFFFAOYSA-N ethyl 4-[2-amino-2-(4-diethoxyphosphorylphenyl)acetyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(=O)C(N)C1=CC=C(P(=O)(OCC)OCC)C=C1 UWELFCKWEVHBGN-UHFFFAOYSA-N 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003527 fibrinolytic agent Substances 0.000 description 1
- 230000003480 fibrinolytic effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- RIKMMFOAQPJVMX-UHFFFAOYSA-N fomepizole Chemical compound CC=1C=NNC=1 RIKMMFOAQPJVMX-UHFFFAOYSA-N 0.000 description 1
- 229960004285 fomepizole Drugs 0.000 description 1
- 238000002695 general anesthesia Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000000025 haemostatic effect Effects 0.000 description 1
- 230000023597 hemostasis Effects 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- COQRGFWWJBEXRC-UHFFFAOYSA-N hydron;methyl 2-aminoacetate;chloride Chemical compound Cl.COC(=O)CN COQRGFWWJBEXRC-UHFFFAOYSA-N 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- DWKPPFQULDPWHX-VKHMYHEASA-N l-alanyl ester Chemical compound COC(=O)[C@H](C)N DWKPPFQULDPWHX-VKHMYHEASA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- LTHGYYYHJIKZED-UHFFFAOYSA-M lithium;2-dimethoxyphosphoryl-2-(phenylmethoxycarbonylamino)acetate Chemical compound [Li+].COP(=O)(OC)C(C([O-])=O)NC(=O)OCC1=CC=CC=C1 LTHGYYYHJIKZED-UHFFFAOYSA-M 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 150000002680 magnesium Chemical class 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- VGIFEXOZPQIHJA-LLVKDONJSA-N methyl (2r)-4-bromo-2-(phenylmethoxycarbonylamino)butanoate Chemical compound COC(=O)[C@@H](CCBr)NC(=O)OCC1=CC=CC=C1 VGIFEXOZPQIHJA-LLVKDONJSA-N 0.000 description 1
- MOCKMZLFLAVJOF-OAHLLOKOSA-N methyl (2r)-4-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)butanoate Chemical compound CCOP(=O)(OCC)CC[C@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 MOCKMZLFLAVJOF-OAHLLOKOSA-N 0.000 description 1
- JVXZHIGNNGLZSZ-LLVKDONJSA-N methyl (2r)-4-hydroxy-2-(phenylmethoxycarbonylamino)butanoate Chemical compound COC(=O)[C@@H](CCO)NC(=O)OCC1=CC=CC=C1 JVXZHIGNNGLZSZ-LLVKDONJSA-N 0.000 description 1
- ZPPZVKOJSVBBSO-MRXNPFEDSA-N methyl (2r)-5-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound CCOP(=O)(OCC)CCC[C@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 ZPPZVKOJSVBBSO-MRXNPFEDSA-N 0.000 description 1
- UIAUGRQODAHAKA-GFCCVEGCSA-N methyl (2r)-5-hydroxy-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound OCCC[C@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 UIAUGRQODAHAKA-GFCCVEGCSA-N 0.000 description 1
- GFPNWJAXDSMFKA-GFCCVEGCSA-N methyl (2r)-5-iodo-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound ICCC[C@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 GFPNWJAXDSMFKA-GFCCVEGCSA-N 0.000 description 1
- HRTQWUHFSXVRPY-NUBCRITNSA-N methyl (2s)-2-amino-3,3-dimethylbutanoate;hydrochloride Chemical compound Cl.COC(=O)[C@@H](N)C(C)(C)C HRTQWUHFSXVRPY-NUBCRITNSA-N 0.000 description 1
- KUGLDBMQKZTXPW-JEDNCBNOSA-N methyl (2s)-2-amino-3-methylbutanoate;hydrochloride Chemical compound Cl.COC(=O)[C@@H](N)C(C)C KUGLDBMQKZTXPW-JEDNCBNOSA-N 0.000 description 1
- SWVMLNPDTIFDDY-FVGYRXGTSA-N methyl (2s)-2-amino-3-phenylpropanoate;hydrochloride Chemical compound Cl.COC(=O)[C@@H](N)CC1=CC=CC=C1 SWVMLNPDTIFDDY-FVGYRXGTSA-N 0.000 description 1
- HJOYIQNIPJCMBN-SNVBAGLBSA-N methyl (2s)-3-diethoxyphosphoryl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate Chemical compound CCOP(=O)(OCC)C[C@H](C(=O)OC)NC(=O)OC(C)(C)C HJOYIQNIPJCMBN-SNVBAGLBSA-N 0.000 description 1
- VGIFEXOZPQIHJA-NSHDSACASA-N methyl (2s)-4-bromo-2-(phenylmethoxycarbonylamino)butanoate Chemical compound COC(=O)[C@H](CCBr)NC(=O)OCC1=CC=CC=C1 VGIFEXOZPQIHJA-NSHDSACASA-N 0.000 description 1
- MOCKMZLFLAVJOF-HNNXBMFYSA-N methyl (2s)-4-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)butanoate Chemical compound CCOP(=O)(OCC)CC[C@@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 MOCKMZLFLAVJOF-HNNXBMFYSA-N 0.000 description 1
- JVXZHIGNNGLZSZ-NSHDSACASA-N methyl (2s)-4-hydroxy-2-(phenylmethoxycarbonylamino)butanoate Chemical compound COC(=O)[C@H](CCO)NC(=O)OCC1=CC=CC=C1 JVXZHIGNNGLZSZ-NSHDSACASA-N 0.000 description 1
- ZPPZVKOJSVBBSO-INIZCTEOSA-N methyl (2s)-5-diethoxyphosphoryl-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound CCOP(=O)(OCC)CCC[C@@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 ZPPZVKOJSVBBSO-INIZCTEOSA-N 0.000 description 1
- UIAUGRQODAHAKA-LBPRGKRZSA-N methyl (2s)-5-hydroxy-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound OCCC[C@@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 UIAUGRQODAHAKA-LBPRGKRZSA-N 0.000 description 1
- GFPNWJAXDSMFKA-LBPRGKRZSA-N methyl (2s)-5-iodo-2-(phenylmethoxycarbonylamino)pentanoate Chemical compound ICCC[C@@H](C(=O)OC)NC(=O)OCC1=CC=CC=C1 GFPNWJAXDSMFKA-LBPRGKRZSA-N 0.000 description 1
- YJEZEMGLLFLMDF-UHFFFAOYSA-N methyl 2-amino-3-methoxybenzoate Chemical compound COC(=O)C1=CC=CC(OC)=C1N YJEZEMGLLFLMDF-UHFFFAOYSA-N 0.000 description 1
- AHAQQEGUPULIOZ-UHFFFAOYSA-N methyl 2-aminobutanoate;hydrochloride Chemical compound Cl.CCC(N)C(=O)OC AHAQQEGUPULIOZ-UHFFFAOYSA-N 0.000 description 1
- AJHZGVMKIXHMNP-UHFFFAOYSA-N methyl 2-anilinoacetate;hydrochloride Chemical compound Cl.COC(=O)CNC1=CC=CC=C1 AJHZGVMKIXHMNP-UHFFFAOYSA-N 0.000 description 1
- GSYSFVSGPABNNL-UHFFFAOYSA-N methyl 2-dimethoxyphosphoryl-2-(phenylmethoxycarbonylamino)acetate Chemical compound COC(=O)C(P(=O)(OC)OC)NC(=O)OCC1=CC=CC=C1 GSYSFVSGPABNNL-UHFFFAOYSA-N 0.000 description 1
- TZJOTDHMGVBGRS-UHFFFAOYSA-N methyl 2-hydroxy-3-propan-2-ylbenzoate Chemical compound COC(=O)C1=CC=CC(C(C)C)=C1O TZJOTDHMGVBGRS-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- OZNYZQOTXQSUJM-UHFFFAOYSA-N n,n'-dicyclohexylmorpholine-4-carboximidamide Chemical compound C1CCCCC1NC(N1CCOCC1)=NC1CCCCC1 OZNYZQOTXQSUJM-UHFFFAOYSA-N 0.000 description 1
- FMJBBSYTZYDJDS-UHFFFAOYSA-N n-(2-oxoethenyl)-2-phenylpyrimidine-4-carboxamide Chemical class O=C=CNC(=O)C1=CC=NC(C=2C=CC=CC=2)=N1 FMJBBSYTZYDJDS-UHFFFAOYSA-N 0.000 description 1
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 1
- HWYVLXXGARLCRX-HNCPQSOCSA-N n-cyclohexylcyclohexanamine;(2r)-4-hydroxy-2-(phenylmethoxycarbonylamino)butanoic acid Chemical compound C1CCCCC1NC1CCCCC1.OCC[C@H](C(O)=O)NC(=O)OCC1=CC=CC=C1 HWYVLXXGARLCRX-HNCPQSOCSA-N 0.000 description 1
- HWYVLXXGARLCRX-PPHPATTJSA-N n-cyclohexylcyclohexanamine;(2s)-4-hydroxy-2-(phenylmethoxycarbonylamino)butanoic acid Chemical compound C1CCCCC1NC1CCCCC1.OCC[C@@H](C(O)=O)NC(=O)OCC1=CC=CC=C1 HWYVLXXGARLCRX-PPHPATTJSA-N 0.000 description 1
- WOOWBQQQJXZGIE-UHFFFAOYSA-N n-ethyl-n-propan-2-ylpropan-2-amine Chemical compound CCN(C(C)C)C(C)C.CCN(C(C)C)C(C)C WOOWBQQQJXZGIE-UHFFFAOYSA-N 0.000 description 1
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- 125000005484 neopentoxy group Chemical group 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000002414 normal-phase solid-phase extraction Methods 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 229950002383 orbofiban Drugs 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
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- 210000001672 ovary Anatomy 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- UQPUONNXJVWHRM-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 UQPUONNXJVWHRM-UHFFFAOYSA-N 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 238000002732 pharmacokinetic assay Methods 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000002571 phosphodiesterase inhibitor Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- PRAYXGYYVXRDDW-UHFFFAOYSA-N piperidin-2-ylmethanol Chemical compound OCC1CCCCN1 PRAYXGYYVXRDDW-UHFFFAOYSA-N 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 238000002616 plasmapheresis Methods 0.000 description 1
- 239000000106 platelet aggregation inhibitor Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 229960004197 prasugrel Drugs 0.000 description 1
- DTGLZDAWLRGWQN-UHFFFAOYSA-N prasugrel Chemical compound C1CC=2SC(OC(=O)C)=CC=2CN1C(C=1C(=CC=CC=1)F)C(=O)C1CC1 DTGLZDAWLRGWQN-UHFFFAOYSA-N 0.000 description 1
- 201000011461 pre-eclampsia Diseases 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- UBKCIXXGQRZHRO-UHFFFAOYSA-N propan-2-yl 2-aminoacetate;hydrochloride Chemical compound Cl.CC(C)OC(=O)CN UBKCIXXGQRZHRO-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- YDBMNSABUROTEK-UHFFFAOYSA-N propyl 2-aminoacetate;hydrochloride Chemical compound Cl.CCCOC(=O)CN YDBMNSABUROTEK-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 1
- JHHZLHWJQPUNKB-UHFFFAOYSA-N pyrrolidin-3-ol Chemical compound OC1CCNC1 JHHZLHWJQPUNKB-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000003259 recombinant expression Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 125000005920 sec-butoxy group Chemical group 0.000 description 1
- FYXHWMQPCJOJCH-GMAHTHKFSA-N selatogrel Chemical compound C1CN(C(=O)OCCCC)CCN1C(=O)[C@H](CP(O)(O)=O)NC(=O)C1=CC(N2C[C@H](CC2)OC)=NC(C=2C=CC=CC=2)=N1 FYXHWMQPCJOJCH-GMAHTHKFSA-N 0.000 description 1
- 229950005747 sibrafiban Drugs 0.000 description 1
- 208000007056 sickle cell anemia Diseases 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000001476 sodium potassium tartrate Substances 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000011537 solubilization buffer Substances 0.000 description 1
- 238000011301 standard therapy Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- NGIGLOKJPWGIJT-QMMMGPOBSA-N tert-butyl (3s)-3-methoxypyrrolidine-1-carboxylate Chemical compound CO[C@H]1CCN(C(=O)OC(C)(C)C)C1 NGIGLOKJPWGIJT-QMMMGPOBSA-N 0.000 description 1
- OSWULUXZFOQIRU-UHFFFAOYSA-N tert-butyl 2-aminoacetate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)CN OSWULUXZFOQIRU-UHFFFAOYSA-N 0.000 description 1
- HGHYERVLYRBRPJ-UHFFFAOYSA-N tert-butyl chloromethyl carbonate Chemical compound CC(C)(C)OC(=O)OCCl HGHYERVLYRBRPJ-UHFFFAOYSA-N 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229940125670 thienopyridine Drugs 0.000 description 1
- 239000002175 thienopyridine Substances 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 239000003868 thrombin inhibitor Substances 0.000 description 1
- 239000003634 thrombocyte concentrate Substances 0.000 description 1
- 206010043554 thrombocytopenia Diseases 0.000 description 1
- 208000014754 thrombocytosis disease Diseases 0.000 description 1
- 230000002537 thrombolytic effect Effects 0.000 description 1
- RZWIIPASKMUIAC-VQTJNVASSA-N thromboxane Chemical compound CCCCCCCC[C@H]1OCCC[C@@H]1CCCCCCC RZWIIPASKMUIAC-VQTJNVASSA-N 0.000 description 1
- OEKWJQXRCDYSHL-FNOIDJSQSA-N ticagrelor Chemical compound C1([C@@H]2C[C@H]2NC=2N=C(N=C3N([C@H]4[C@@H]([C@H](O)[C@@H](OCCO)C4)O)N=NC3=2)SCCC)=CC=C(F)C(F)=C1 OEKWJQXRCDYSHL-FNOIDJSQSA-N 0.000 description 1
- 229960002528 ticagrelor Drugs 0.000 description 1
- 229960005001 ticlopidine Drugs 0.000 description 1
- PHWBOXQYWZNQIN-UHFFFAOYSA-N ticlopidine Chemical compound ClC1=CC=CC=C1CN1CC(C=CS2)=C2CC1 PHWBOXQYWZNQIN-UHFFFAOYSA-N 0.000 description 1
- COKMIXFXJJXBQG-NRFANRHFSA-N tirofiban Chemical compound C1=CC(C[C@H](NS(=O)(=O)CCCC)C(O)=O)=CC=C1OCCCCC1CCNCC1 COKMIXFXJJXBQG-NRFANRHFSA-N 0.000 description 1
- 229960003425 tirofiban Drugs 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- CICLIHWCPPVFQE-SEUOVDNZSA-N tributyl-[(1s,2r)-2-(methoxymethyl)cyclopropyl]stannane Chemical compound CCCC[Sn](CCCC)(CCCC)[C@H]1C[C@@H]1COC CICLIHWCPPVFQE-SEUOVDNZSA-N 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 229940019333 vitamin k antagonists Drugs 0.000 description 1
- 229960005080 warfarin Drugs 0.000 description 1
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 description 1
- 229950004893 xemilofiban Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657181—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
- C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
- C07F9/65846—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring the phosphorus atom being part of a six-membered ring which may be condensed with another ring system
Definitions
- the present invention relates to certain phosphonic acid derivatives and their use as P2Yi2 receptor antagonists in the treatment and/or prevention of peripheral vascular, of visceral-, hepatic- and renal-vascular, of cardiovascular and of cerebrovascular diseases or conditions associated with platelet aggregation, including thrombosis in humans and other mammals.
- Haemostasis is referred to as the natural balance of maintaining the fluidity of the blood in the vascular system and preventing excessive blood loss subsequent to blood vessel injury by rapid formation of a solid blood clot. After vascular damage, contraction of the vessels and platelet adhesion occur immediately followed by aggregation of the platelets, activation of the coagulation cascade and finally also of the fibrinolytic system. Haemostatic abnormalities can lead to excessive bleeding or thrombosis, both life -threatening situations.
- antiplatelet agents have been developed over the past several years based on different mechanisms of action.
- the most widely used agent in antiplatelet therapy is aspirin, which irreversibly inhibits cyclooxygenase-1 and thereby affecting the thromboxane pathway.
- aspirin Although not optimally efficacious, treatment with aspirin remains the standard therapy against which new therapeutics are compared and judged.
- GPIIb/IIIa receptor antagonists e.g. abciximab, eptifibatide, and tirofiban blocking platelet aggregation are available on the market.
- some orally active GPIIb/IIIa antagonists e.g. sibrafiban, xemilofiban or orbofiban have not been successful in clinical development so far.
- Adenosine 5 '-diphosphate is a key mediator in platelet activation and aggregation interfering with two platelet ADP receptors P2Yi and P2Yi2.
- Antagonists of the platelet ADP receptor have been identified and display inhibition of platelet aggregation and antithrombotic activity.
- the most effective antagonists known so far are the thienopyridines ticlopidine, clopidogrel and CS-747, which have been used clinically as antithrombotic agents. It could be shown that these drugs, via their reactive metabolites, irreversibly block the ADP receptor subtype P2Yi 2 .
- P2Yi 2 antagonists like AR-C69931MX (Cangrelor) or AZD6140 have reached phase II clinical studies. These inhibitors are selective platelet ADP receptor antagonists, which inhibit ADP-dependent platelet aggregation, and are effective in vivo.
- Piperazino-carbonylmethylaminocarbonyl-naphtyl or -quinolyl derivatives have been described as ADP receptor antagonists in WO 02/098856 and WO 2004/052366.
- WO 2006/114774 describes 2-phenyl-4-(carbonylmethylaminocarbonyl)-pyrimidine derivatives as P2Yi 2 receptor antagonists. However these compounds do not contain any phosphonic acid or phosphonate motif.
- R represents phenyl, wherein the phenyl is unsubstituted or substituted 1 to 3 times (preferably unsubstituted or substituted once or twice, more preferably unsubstituted or substituted once and most preferably unsubstituted) by substituents each independently selected from the group consisting of halogen, methyl, methoxy, trifiuoromethyl and trifluoromethoxy;
- W represents a bond
- R 2 represents alkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, aryl or heteroaryl; or
- W represents -O- and R 2 represents alkyl, cycloalkyl, hydroxyalkyl or heterocyclyl; or
- W represents -NR 3 -
- R 2 represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R represents hydrogen or alkyl
- W represents -NR - and R and R form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said - A - heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O-, -S-, -CO- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy and R y representing
- R 5 represents hydroxy or unsubstituted phenyloxy
- P(O)R R represents a group selected from the following structures
- R 6 represents hydrogen or (Ci-C 3 )alkyl
- R 7 represents (Ci-C 4 )alkyl or unsubstituted (C 3 -C 6 )cycloalkyl
- R 9 represents (Ci-C 4 )alkyl
- R 10 represents hydrogen, (Ci-C4)alkyl, unsubstituted phenyl or unsubstituted benzyl
- R 11 represents hydrogen, (Ci-C4)alkyl or (Ci-C4)alkoxy; and to the salts (in particular pharmaceutically acceptable salts) of such compounds.
- the compounds of formula I may contain one or more stereogenic or asymmetric centers, such as one or more asymmetric carbon atoms.
- the compounds of formula I may thus be present as mixtures of stereoisomers or preferably as pure stereoisomers. Mixtures of stereoisomers may be separated in a manner known to a person skilled in the art.
- the compounds of formula I are P2Yi2 receptor antagonists. Accordingly, they are useful in therapy (including combination therapy), where they can be widely used as inhibitors of platelet activation, aggregation and degranulation, as promoters of platelet disaggregation or as anti-thrombotic agents.
- halogen refers to fluorine, chlorine, bromine or iodine, preferably to fluorine, chlorine or bromine and more preferably to fluorine.
- alkyl refers to a saturated straight or branched chain alkyl group containing 1 to 7 carbon atoms (e.g. methyl, ethyl, ⁇ -propyl, ⁇ -propyl,
- ⁇ -heptyl or ⁇ -heptyl and preferably 1 to 4 carbon atoms.
- preferred alkyl groups include methyl, ethyl, ⁇ -propyl, ⁇ o-propyl, «-butyl, ⁇ o-butyl, sec-butyl and tert-butyl.
- (C x -C y )alkyl (x and y being integers) refers to a straight or branched chain alkyl group containing x to y carbon atoms.
- alkoxy refers to a saturated straight or branched chain alkoxy group containing 1 to 6 carbon atoms (e.g. methoxy, ethoxy, «-propoxy, ⁇ o-propoxy, «-butoxy, ⁇ o-butoxy, sec-butoxy, tert-butoxy, «-pentoxy, neopentyloxy, ⁇ o-pentyloxy, «-hexyloxy or ⁇ o-hexyloxy), and preferably 1 to 4 carbon atoms.
- alkoxy groups include methoxy, ethoxy, «-propoxy, ⁇ o-propoxy, «-butoxy, ⁇ o-butoxy, sec-butoxy and tert-butoxy.
- (C x -C y )alkoxy (x and y being integers) refers to a straight or branched chain alkoxy group containing x to y carbon atoms.
- hydroxy alkyl refers to an alkyl group as previously defined wherein one hydrogen atom has been replaced by a hydroxy (i.e. -OH) group.
- hydroxy alkyl groups include, but are not limited to, hydroxymethyl, 2-hydroxy-ethyl, 2-hydroxy-propyl, 2-hydroxy-l -methyl-ethyl, 2-hydroxy- 1 , 1 -dimethyl-ethyl, 1 -hydroxy- propyl, 3-hydroxy -propyl, 1 -hydroxy -butyl, 3-hydroxy-butyl, 4-hydroxy -butyl, 3-hydroxy- pentyl and 3-hydroxy-3-methyl-butyl (and preferably hydroxymethyl, 2-hydroxy-ethyl and 3 -hy droxy-butyl) .
- alkoxyalkyl refers to an alkyl group as previously defined wherein one hydrogen atom has been replaced by an alkoxy group as previously defined.
- alkoxyalkyl groups include, but are not limited to, 3-methoxy-propyl, methoxymethyl and 2-methoxy-ethyl (and notably methoxymethyl and 2-methoxy-ethyl).
- alkoxymethyl means for example methoxymethyl or 2-methoxy- ethyl.
- cycloalkyl refers to a saturated cyclic hydrocarbon moiety containing 3 to 7 carbon atoms which may be unsubstituted or substituted once by hydroxy, hydroxymethyl, alkoxymethyl (preferably methoxymethyl or ethoxymethyl and more preferably methoxymethyl) or alkoxy (preferably methoxy or ethoxy and more preferably methoxy).
- cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 4-hydroxy-cyclohexyl, 2-hydroxy-cyclohexyl, 2-hydroxymethyl-cyclopropyl and 2- methoxymethyl-cyclopropyl (in particular cyclopropyl, 2-hydroxymethyl-cyclopropyl and
- alkoxycarbonylalkyl groups include, but are not limited to, 2-ethoxycarbonyl-ethyl and
- carboxyalkyl refers to an alkyl group as previously defined wherein one hydrogen atom has been replaced by a carboxy group (that is, by a -COOH group).
- carboxylalkyl groups include, but are not limited to,
- aryl refers to an aromatic cyclic group with one, two or three rings, having from 6 to 14 carbon ring-atoms and preferably from 6 to 10 carbon ring-atoms, for example to phenyl or naphthyl groups (and notably to phenyl groups).
- Any aryl group (and in particular any phenyl group) as defined herein may be unsubstituted or substituted with one, two or more substituents (preferably with one to three substituents, more preferably with one or two substituents and notably with one substituent), each independently selected from the group consisting of halogen, alkyl and alkoxy.
- substituents preferably with one to three substituents, more preferably with one or two substituents and notably with one substituent
- Specific examples of aryl groups are phenyl, 2-fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2-chlorophenyl,
- aralkyl refers to an aryl group appended to the parent molecular moiety through an alkyl group wherein however the aryl group may be unsubstituted or substituted with 1 to 3 substituents selected independently from the group consisting of halogen, alkyl and alkoxy.
- substituents selected independently from the group consisting of halogen, alkyl and alkoxy.
- Representative examples of aralkyl groups include, but are not limited to, benzyl, 2-phenylethyl, 3-phenylpropyl and 2-naphth-2-ylethyl.
- Preferred aralkyl groups are the phenylalkyl groups.
- phenylalkyl refers to an unsubstituted phenyl group appended to the parent molecular moiety through an alkyl group.
- phenylalkyl groups include, but are not limited to, benzyl, 2-phenylethyl and 3-phenylpropyl. Preferred is benzyl.
- heteroaryl refers to a mono-, bi- or tricyclic aromatic ring system containing up to 14 ring atoms wherein at least one of the rings contains at least one heteroatom independently selected from the group consisting of nitrogen, oxygen and sulfur; in addition, the term “heteroaryl” may also refer to 1-oxy- pyridinyl groups.
- the heteroaryl group can be unsubstituted or substituted with 1 to 3 substituents (preferably 1 to 2 substituents and more preferably 1 substituent) selected independently from the group consisting of halogen, alkyl, alkoxy, trifluoromethyl and trifluoromethoxy.
- heteroaryl groups include, but are not limited to, thienyl, furanyl, pyrrolyl, pyrazolyl, thiazolyl, imidazolyl, oxazolyl, pyridinyl, 1 -oxy-4-pyridinyl, l-oxy-3 -pyridinyl, 1 -oxy-2-pyridinyl, pyrimidinyl, quinolinyl, benzimidazolyl, benzo thiazolyl, benzothienyl, benzoxazolyl, benzofuranyl, indolyl, carbazolyl, phenothiazinyl and phenoxazinyl (preferably thienyl, pyrazolyl and 4-methyl- pyrazolyl).
- monocyclic heteroaryl refers to a monocyclic aromatic ring system containing 5 or 6 ring atoms among which 1 or 2 may be heteroatoms selected from O, N and S.
- the monocyclic heteroaryl group can be unsubstituted or substituted with 1 to 2 substituents (preferably 1 substituent) selected independently from the group consisting of halogen, alkyl, alkoxy, trifluoromethyl and trifluoromethoxy.
- monocyclic heteroaryl groups include, but are not limited to, thienyl, furanyl, pyrrolyl, pyrazolyl, thiazolyl, imidazolyl, oxazolyl, pyridinyl and pyrimidinyl.
- heterocyclyl refers to an unsubstituted saturated monocyclic moiety of 3 to 7 ring members containing 1 to 2 heteroatoms selected from nitrogen, oxygen and sulfur, it being however understood that (i) a heterocyclyl group is not attached to the rest of the molecule by a nitrogen atom, (ii) a heterocyclyl group of 3 or 4 ring members contains only one heteroatom which is a nitrogen atom and (iii) a heterocyclyl group does not contain 2 sulfur atoms.
- the sulfur atom of a heterocyclyl group may be in an oxidised form, i.e. as a sulfoxide or sulfonyl.
- heterocyclyl groups include, but are not limited to, azetidinyl, pyrrolidinyl, tetrahydrofuranyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl (preferably tetrahydrofuran-3-yl).
- variably attached bonds may be used for substituents or groups.
- the substituent or group is attached to either atom linked by the bond into which the variably attached bond is drawn into.
- the compound drawn below is meant that the substituent or group is attached to either atom linked by the bond into which the variably attached bond is drawn into.
- pharmaceutically acceptable salts refers to non-toxic, inorganic or organic acid and/or base addition salts. Reference can be made to "Salt selection for basic drugs", Int. J. Pharm. (1986), 33, 201-217.
- room temperature refers to a temperature of 25°C.
- the term "about” placed before a numerical value "X” refers in the current application to an interval extending from X minus 10% of X to X plus 10% of X, and preferably to an interval extending from X minus 5% of X to X plus 5% of X.
- the term “about” (or alternatively the term “around") placed before a temperature "Y” refers in the current application to an interval extending from the temperature Y minus 10 0 C to Y plus 10 0 C, and preferably to an interval extending from Y minus 5 0 C to Y plus 5 0 C.
- the invention relates to compounds of formula I that are also compounds of formula ICE
- R represents phenyl, wherein the phenyl is unsubstituted or monosubstituted with halogen, methyl or trifluoromethyl;
- W represents a bond
- R 2 represents alkyl, hydro xyalkyl (notably 3-hydroxy-butyl), alkoxyalkyl (notably 3-methoxy-propyl), a cycloalkyl group of 3 to 7 carbon atoms (preferably of 3 to 6, more preferably of 3 to 5 carbon atoms and most preferably of 3 carbon atoms) which may be substituted once by hydroxymethyl or alkoxymethyl (preferably methoxymethyl or ethoxymethyl and more preferably methoxymethyl), a phenyl group which is unsubstituted or monosubstituted with alkoxy, or an unsubstituted monocyclic heteroaryl group; or
- W represents -O- and R 2 represents alkyl (notably methyl), cycloalkyl (notably cyclopentyl), hydroxyalkyl (notably 2-hydroxyethyl) or heterocyclyl (notably tetrahydrofuran-3-yl); or W represents -NR 3 -, R 2 represents alkyl, alkoxycarbonylalkyl [notably 2-(ethoxycarbonyl)- ethyl], carboxyalkyl (notably 2-carboxy-ethyl), hydroxyalkyl (notably 2-hydroxy-ethyl), alkoxyalkyl, heterocyclyl (notably teterahydrofuran-3-yl), cycloalkyl (notably cyclopropyl), phenyl or phenylalkyl (notably benzyl) and R represents hydrogen or alkyl (notably methyl); or W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7
- R a represents hydrogen or methyl
- R 4 represents alkoxy (preferably ethoxy or «-butoxy); n represents 0, 1, 2 or 3, V represents a bond, and m represents 0; or n represents 0 or 1, V represents phenyl, and m represents 0; or n represents 1 , V represents phenyl, and m represents 1 ;
- P(O)R 5 R 8 represents a group selected from the following structures
- R 6 represents hydrogen or (Ci-C 3 )alkyl (preferably hydrogen or methyl);
- R 7 represents (Ci-C 4 )alkyl or unsubstituted (C 3 -C 6 )cycloalkyl;
- R 9 represents (Ci-C 4 )alkyl;
- R 10 represents hydrogen, (Ci-C 4 )alkyl, unsubstituted phenyl or unsubstituted benzyl;
- R 11 represents hydrogen, (Ci-C 4 )alkyl or (Ci-C 4 )alkoxy; and to the salts (in particular pharmaceutically acceptable salts) of such compounds.
- the invention relates to compounds of formula I that are also compounds of formula Ip formula Ip wherein
- R 1 represents phenyl optionally substituted 1 to 3 times (preferably optionally substituted once or twice and more preferably optionally substituted once) by substituents each independently selected from the group consisting of halogen, methyl, methoxy, trifiuoromethyl and trifluoromethoxy;
- W represents a bond
- R 2 represents alkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, aryl or heteroaryl; or
- W represents -O- and R 2 represents alkyl or heterocyclyl
- W represents -NR 3 -
- R 2 represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R represents hydrogen or alkyl; or
- W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and
- heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O-, -S-, -CO- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy and R y representing hydrogen or alkyl; or also W represents -NR - and R and R form, together with the nitrogen that carries them, an imidazolyl, pyrazolyl, 1 ,2,3-triazolyl or 1,2,4-triazolyl ring, which ring may be substituted by an alkyl group (especially by a methyl group);
- R a represents hydrogen or methyl
- R b represents hydrogen or methyl
- R 7 represents (Ci-C 4 )alkyl; and to the salts (in particular pharmaceutically acceptable salts) of such compounds.
- the invention relates to compounds of formula I P that are also compounds of formula IC EP
- R represents phenyl optionally substituted once or twice by substituents independently selected from the group consisting of halogen, methyl, methoxy, trifiuoromethyl and trifluoromethoxy (and preferably optionally substituted once or twice by substituents independently selected from the group consisting of halogen, methyl and trifluoromethyl, especially optionally substituted once by halogen, methyl or trifluoromethyl);
- W represents a bond
- R 2 represents alkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, a phenyl group optionally substituted once by alkoxy, or also an unsubstituted monocyclic heteroaryl group; or
- W represents -O- and R 2 represents alkyl (notably methyl) or heterocyclyl (notably tetrahydrofuran-3-yl); or
- W represents -NR 3 -
- R 2 represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, phenyl or phenylalkyl, or a cycloalkyl group of 3 to 7 carbon atoms (preferably of 3 to 6 and more preferably of 3 to 5 carbon atoms) which may be substituted once by hydroxymethyl or alkoxymethyl (preferably methoxymethyl or ethoxymethyl and more preferably methoxymethyl), and R represents hydrogen or alkyl (and notably hydrogen or methyl); or W represents -NR - and R and R form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members (and notably of 5 to 6 members) wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O- and -NR y -, it being understood however that said heterocycl
- the compounds of formula I as defined in embodiment 1) or 2) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that they are also compounds of formula I STI and have the stereochemistry drawn below
- the compounds of formula I as defined in embodiment 1) or 2) or their salts will be such that they are also compounds of formula Is ⁇ 2 , wherein n represents 1 or 3, and have the stereochemistry drawn below
- the compounds of formula I as defined in embodiment 1), 2) or 5) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that V represents a bond.
- the compounds of formula I as defined in embodiment 1), 2) or 5) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that V represents phenyl.
- the compounds of formula I as defined in embodiment 1), 2), 5) or 7) or their salts will be such that when V represents a bond, then m represents 0 and n represents 1, 2 or 3.
- the compounds of formula I as defined in embodiment 1), 2), 5) or 8) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that when V represents phenyl, then m represents 0 and n represents 0 or 1.
- the compounds of formula I as defined in embodiment 1), 2), 5) or 8) or their salts will be such that when V represents phenyl, then m represents 1 and n represents 1.
- the compounds of formula I as defined in any one of embodiments 1), 2), 5), 7) or 9) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that when n represents 2, V represents a bond and m represents 0, then R represents (C4-Ce)alkoxy, especially linear (C4-Ce)alkoxy and in particular «-butoxy.
- the compounds of formula Ip as defined in embodiment 3) or 4) above or their salts will be such that when n represents 2, then R represents (C4-Ce)alkoxy, especially linear (C4-C ⁇ )alkoxy and in particular «-butoxy.
- the compounds of formula I as defined in any one of embodiments 1) to 5), 7), 8) or 10) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that n represents 0.
- the compounds of formula I as defined in any one of embodiments 1 ) to 11) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that n represents 1.
- the compounds of formula I as defined in any one of embodiments 1) to 5), 7), 9) or 12) to 13) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that n represents 2.
- the compounds of formula I P as defined in embodiment 3) or 4) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that n represents 2.
- the compounds of formula I as defined in embodiment 1), 2), 5), 6), 7) or 9) or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that n represents 3.
- the compounds of formula I as defined in any one of embodiments 1) to 18) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R 4 represents (C4-Ce)alkoxy, especially linear (C4-Ce)alkoxy and in particular n- butoxy.
- the compounds of formula Ip as defined in embodiment 17) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R represents (C4-Ce)alkoxy, especially linear (C4-Ce)alkoxy and in particular «-butoxy.
- the compounds of formula Ip as defined in embodiment 17) or 20) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that they have the stereochemistry drawn below
- the compounds of formula I as defined in one of embodiments 1) to 21) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R represents phenyl optionally substituted once by halogen, methyl, methoxy, trifiuoromethyl or trifluoromethoxy (notably phenyl optionally substituted once by halogen, methyl or trifiuoromethyl and especially phenyl optionally substituted once by fluorine, methyl or trifluoromethyl).
- the compounds of formula I as defined in one of embodiments 1) to 22) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R 1 represents unsubstituted phenyl.
- the compounds of formula I as defined in one of embodiments 1) to 23) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that W represents a bond.
- the compounds of formula I as defined in embodiment 24) above or their salts will be such that R represents alkyl (notably methyl and isopropyl and especially methyl), hydroxyalkyl (especially 3 -hydroxy -butyl), alkoxyalkyl (especially 3-methoxy -propyl), cycloalkyl (especially cyclopropyl optionally substituted once by hydroxymethyl or alkoxymethyl), a phenyl group optionally substituted once by alkoxy, or also an unsubstituted monocyclic heteroaryl group (especially thiophen-3-yl).
- R represents alkyl (notably methyl and isopropyl and especially methyl), hydroxyalkyl (especially 3 -hydroxy -butyl), alkoxyalkyl (especially 3-methoxy -propyl), cycloalkyl (especially cyclopropyl optionally substituted once by hydroxymethyl or alkoxymethyl), a phenyl group optionally substituted once by alkoxy, or also an
- R represents hydroxyalkyl, alkoxyalkyl or cycloalkyl (especially cyclopropyl optionally substituted once by alkoxymethyl or alkoxy and more especially cyclopropyl optionally substituted once by alkoxymethyl).
- W represents -O- and R represents alkyl (notably methyl), cycloalkyl (notably cyclopentyl), hydroxyalkyl (notably 2-hydroxyethyl) or heterocyclyl (notably tetrahydrofuran-3-yl).
- the compounds of formula I as defined in one of embodiments 1) to 23) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that W represents -O- .
- the compounds of formula I as defined in embodiment 28) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R represents methyl or heterocyclyl (e.g. tetrahydrofuran-3-yl), and notably heterocyclyl (especially tetrahydrofuran-3-yl).
- the compounds of formula I as defined in one of embodiments 1), 3) or 5) to 23) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that W represents -NR -, R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R 3 represents hydrogen or alkyl, or such that W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -
- the compounds of formula I as defined in one of embodiments 1) to 3) or 5) to 23) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that W represents -NR -, R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, phenyl or phenylalkyl and R represents hydrogen or alkyl; or such that W represents -NR - and R and R form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members (preferably 4 to 6 members) wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X
- the compounds of formula I as defined in embodiment 30) above or their salts will be such that W represents -NR -, R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R 3 represents hydrogen or alkyl (notably hydrogen or methyl).
- the compounds of formula I as defined in embodiment 31) or 32) above or their salts will be such that W represents -NR -, R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl or phenylalkyl and R represents hydrogen or alkyl (notably hydrogen or methyl).
- the compounds of formula I as defined in embodiment 31) or 32) above or their salts will be such that W represents -NR 3 -, R 2 represents (Ci-C4)alkyl, (Ci-C2)alkoxy-carbonyl-(Ci- C 4 )alkyl, carboxy-(Ci-C 4 )alkyl, (Ci-C 4 )hydroxyalkyl, (Ci-C 2 )alkoxy-(Ci-C 4 )alkyl, heterocyclyl, cycloalkyl or phenylalkyl (and in particular methyl, ethyl, ⁇ o-propyl, 2- ethoxycarbonyl-ethyl, 2-carboxy-ethyl, 2-hydroxyethyl, 2-methoxy-ethyl, tetrahydrofuran-3- yl, cyclopropyl or benzyl) and R 3 represents hydrogen
- the compounds of formula I as defined in embodiment 30) above or their salts will be such that W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O-, -S-, -CO- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy and R y representing hydrogen or alkyl (notably hydrogen or methyl).
- the compounds of formula I as defined in embodiment 31) or 35) above or their salts will be such that W represents -NR - and R and R form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members (and notably of 4 to 6 members and especially of 5 to 6 members) wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy (and notably hydroxy, hydroxymethyl or alkoxy) and R y representing alkyl (especially methyl).
- the compounds of formula I as defined in embodiment 31) or 35) above or their salts will be such that W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 6 members (and especially of 5 to 6 members) wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O- and -NR y -, R x representing hydroxy, hydroxymethyl, methoxymethyl or methoxy (especially hydroxy, hydroxymethyl or methoxy) and R y representing methyl (and especially such that R and R form, together with the nitrogen that carries them, 3-methoxymethyl-azetidin-l-
- the compounds of formula I as defined in embodiment 30) above or their salts will be such that W represents -NR - and R and R form, together with the nitrogen that carries them, an imidazolyl, pyrazolyl, 1 ,2,3-triazolyl or 1 ,2,4-triazolyl ring, which ring may be substituted by an alkyl group (especially by a methyl group).
- the compounds of formula I as defined in embodiment 31) or 38) above or their salts will be such that R and R form, together with the nitrogen that carries them, a pyrazolyl ring which may be substituted by a methyl group (and in particular such that R and R form, together with the nitrogen that carries them, pyrazol-1-yl or 4-methyl-pyrazol-l-yl).
- the compounds of formula I as defined in one of embodiments 1) to 11), 14) to 18) or 21) to 39) above will preferably be such that R represents (C2-C4)alkoxy, especially linear (C2-C4)alkoxy, in particular ethoxy or «-butoxy.
- the compounds of formula I (among which the pharmaceutically acceptable salts will be preferred) will be such that R represents ethoxy.
- One main embodiment of this invention relates to the compounds of formula I P as defined in embodiment 3) that are also compounds of formula I PD
- R 1 represents phenyl optionally substituted 1 to 3 times (preferably optionally substituted once or twice and more preferably optionally substituted once) by substituents each independently selected from the group consisting of halogen, methyl, methoxy, trifiuoromethyl and trifluoromethoxy;
- W represents a bond
- R represents alkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, aryl or heteroaryl;
- W represents -O- and R represents alkyl or heterocyclyl
- W represents -NR -, R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R 3 represents hydrogen or alkyl; or
- W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and
- heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O-, -S-, -CO- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy and R y representing hydrogen or alkyl; or also W represents -NR - and R and R form, together with the nitrogen that carries them, an imidazolyl, pyrazolyl, 1,2,3-triazolyl or 1,2,4-triazolyl ring, which ring may be substituted by an alkyl group (especially by a methyl group);
- R a represents hydrogen or methyl
- R b represents hydrogen or methyl
- R 4 represents alkoxy; n represents 0, 1 or 2; and to the salts (in particular pharmaceutically acceptable salts) of such compounds.
- Another main embodiment of this invention relates to the compounds of formula Ip as defined in embodiment 3) that are also compounds of formula I P _ PDG wherein
- R 1 represents phenyl optionally substituted 1 to 3 times (preferably optionally substituted once or twice and more preferably optionally substituted once) by substituents each independently selected from the group consisting of halogen, methyl, methoxy, trifiuoromethyl and trifluoromethoxy;
- W represents a bond, and R 2 represents alkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, aryl or heteroaryl; or W represents -O- and R 2 represents alkyl or heterocyclyl; or
- W represents -NR -
- R represents alkyl, alkoxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, alkoxyalkyl, heterocyclyl, cycloalkyl, aryl or aralkyl and R 3 represents hydrogen or alkyl; or W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 4 to 7 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 -, -CHR X -, -O-, -S-, -CO- and -NR y -, it being understood however that said heterocyclic ring does not contain more than one member selected from the group consisting of -CHR X -, -O-, -S-, -CO- and -NR y -, R x representing hydroxy, hydroxymethyl, alkoxymethyl or alkoxy and R y representing hydrogen or al
- the compounds of formula Ip as defined in embodiment 44) above or their salts will be such that R represents hydrogen (and notably such that R 5 represents 2,2-dimethyl-propionyloxymethoxy or isobutyryloxymethoxy).
- the compounds of formula I as defined in any one of embodiments 1) to 43) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that R 5 and, if present, R 8 are identical and represent hydroxy.
- the compounds of formula I as defined in any one of embodiments 1), 2), 5) to 12), 14) to 16), 18), 19) or 22) to 42) above or their salts (among which the pharmaceutically acceptable salts will be preferred) will be such that P(O)R 5 R 8 represents a group selected from the following structures
- R 1 represents phenyl
- W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a heterocyclic ring of 5 members wherein the members needed to complete said heterocyclic ring are each independently selected from -CH 2 - and -CHR X -, it being understood however that said heterocyclic ring does not contain more than one -CHR X - group, R x representing alkoxy (and preferrably W represents -NR 3 - and R 2 and R 3 form, together with the nitrogen that carries them, a 3-methoxy-pyrrolidin-l-yl group);
- R a represents hydrogen
- R b represents hydrogen
- P(O)R R represents a group selected from the following structures
- R 6 represents hydrogen
- R 7 represents (Ci-C 4 )alkyl
- R 9 represents (Ci-C 4 )alkyl
- R 10 represents hydrogen, (Ci-C 4 )alkyl or unsubstituted phenyl; and to the salts (in particular pharmaceutically acceptable salts) of such compounds. 55)
- the following compounds of formula I as defined in embodiment 1) to 4) are particularly preferred:
- a further object of the invention is the compounds of formula I (or of formula I CE ) as defined in one of embodiments 1) to 56) above, or their pharmaceutically acceptable salts, as medicaments.
- the compounds of formula I and their pharmaceutically acceptable salts can be used as medicaments, e.g. in the form of pharmaceutical compositions for enteral or parental administration.
- the invention thus also relates to pharmaceutical compositions containing at least one compound according to one of embodiments 1) to 56) above, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent or excipient.
- the invention relates to pharmaceutical compositions containing at least one compound of formula I (or of formula I CE ) and one or more pharmaceutically acceptable carriers, diluents or excipients.
- compositions can be effected in a manner which will be familiar to any person skilled in the art (see for example Remington, The Science and Practice of Pharmacy, 21st Edition (2005), Part 5, "Pharmaceutical Manufacturing” [published by Lippincott Williams & Wilkins]) by bringing the described compounds of formula I or their pharmaceutically acceptable salts, optionally in combination with other therapeutically valuable substances, into a galenical administration form together with suitable, non-toxic, inert, therapeutically compatible solid or liquid carrier materials and, if desired, usual pharmaceutical adjuvants.
- ⁇ ⁇ ⁇ for the treatment or prophylaxis of diseases including stable angina, unstable angina, myocardial infarction, embolism (including complications of atherosclerosis, notably embolic stroke), arterial thrombosis (including primary arterial thrombotic complications of atherosclerosis, notably thrombotic stroke), venous thrombosis (notably deep vein thrombosis), thrombosis secondary to vascular damage or to inflammation (including vasculitis, arteritis and glomerulonephritis), venoocclusive diseases, transient ischaemic attacks, peripheral vascular diseases, myocardial infarction with or without thrombolysis, myeloproliferative disease, thrombocythaemia, sickle cell disease, inflammatory bowel disease, thrombotic thrombocytopaenic purpura, haemolytic uraemic syndrome; ⁇ ⁇ for preventing thrombotic complications of septicaemia, adult respiratory distress syndrome, anti-phospholipid
- a particular object of this invention is the use of a compound of formula I (or of formula I CE ) as defined in one of embodiments 1) to 56) above, or of a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the uses listed in embodiment 59) above, and for the manufacture of a medicament for the treatment of occlusive vascular disorders in general.
- the invention relates to the use of a compound of formula I (or of formula I CE ) as defined in one of embodiments 1) to 56) above, or of a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment and/or prevention of occlusive vascular disorders as well as to the use of a compound of formula I (or of formula I CE ) for the manufacture of a medicament for the treatment and/or prevention of peripheral vascular, of visceral-, hepatic- and renal-vascular, of cardiovascular and of cerebrovascular diseases or conditions associated with platelet aggregation, including thrombosis in humans and other mammals.
- the invention further relates to the use of a compound of formula I (or of formula I CE ) according to one of embodiments 1) to 56) above, or of a pharmaceutically acceptable salt thereof, for the preservation of blood products in vitro (e.g. the preservation of platelet concentrates), or for the prevention of occlusion in extra-corporeal blood or blood product treatment machines (such as renal dialysis machines or plasmapheresis machines).
- a compound of formula I or of formula I CE ) according to one of embodiments 1) to 56) above, or of a pharmaceutically acceptable salt thereof, for the preservation of blood products in vitro (e.g. the preservation of platelet concentrates), or for the prevention of occlusion in extra-corporeal blood or blood product treatment machines (such as renal dialysis machines or plasmapheresis machines).
- the invention also relates to methods of treatment for the disorders mentioned in embodiment 59) above, said methods comprising the administration to a patient in need thereof of an effective amount of a compound of formula I (or of formula I CE ) according to one of embodiments 1) to 56), or of a pharmaceutically acceptable salt of such a compound.
- any reference to a compound of formula I, ICE, Ip, ICEP, ISTI, IST2, IPD or IP_PDG in this text is to be understood as referring also to the salts (and especially the pharmaceutically acceptable salts) of such compounds, as appropriate and expedient.
- PEG400 polyethylene glycol with a molecular weight of 400 g/mol
- a further aspect of the invention is a process for the preparation of compounds of formula (I) (or formula I CE ).
- Compounds of formula (I) of the present invention can be prepared according to the general sequence of reactions outlined in the schemes below wherein V, W, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , n, m and q are as defined for formula (I).
- the compounds obtained may also be converted into pharmaceutically acceptable salts thereof in a manner known per se.
- the compounds of formula I D can be prepared by treating the compounds of formula II with HCl optionally in the presence of water, in a suitable organic solvent such as THF, EA, dioxane or Et 2 O and preferably at a temperature around RT, or with trimethylsilyl bromide or trimethylsilyl iodide in a suitable solvent such as DCM or MeCN and preferably at a temperature around RT.
- a suitable organic solvent such as THF, EA, dioxane or Et 2 O and preferably at a temperature around RT
- trimethylsilyl bromide or trimethylsilyl iodide in a suitable solvent such as DCM or MeCN and preferably at a temperature around RT.
- a suitable base e.g. NEt 3 , DIPEA, DCMC
- suitable solvent such as DMF, NMP or DMPU
- a suitable base e.g. NEt 3
- an activating mixture of reagents such as a combination of 2,2'- dipyridyl disulfide and PPh 3 in a suitable solvent such as anhydrous pyridine and preferably at a temperature of about 60 0 C.
- a condensing reagent e.g. PyBOP
- the respective compounds of formula I PDG can be prepared in a three-step procedure starting from the respective phosphonic acid of formula I D : 1. a coupling reaction is performed with a phenol in the presence of a condensing reagent (e.g. PyBOP) and a suitable base (e.g. NEt 3 , DIPEA) in a suitable solvent such as DMF and preferably at a temperature between RT and 45°C;
- a condensing reagent e.g. PyBOP
- a suitable base e.g. NEt 3 , DIPEA
- a saponification reaction is performed using standard conditions such as NaOH in a mixture of water and a suitable organic solvent such as MeOH or EtOH; and finally
- a suitable base e.g. NEt 3
- an activating mixture of reagents such as a combination of 2,2'-dipyridyl disulfide and PPh 3
- a suitable solvent such as anhydrous pyridine and preferably at a temperature of about 60 0 C.
- the compounds of formula I PDG can be prepared in a two-step procedure starting from the respective phosphonic acid of formula I D :
- a coupling reaction is performed with benzyl alcohol in the presence of a suitable base (e.g. NEt 3 ) and an activating mixture of reagents such as a combination of 2,2'-dipyridyl disulfide and PPh 3 in a suitable solvent such as anhydrous pyridine and preferably at a temperature of about 60 0 C to give the mono-benzylated intermediate; and
- a suitable base e.g. NEt 3
- an activating mixture of reagents such as a combination of 2,2'-dipyridyl disulfide and PPh 3
- a suitable solvent such as anhydrous pyridine and preferably at a temperature of about 60 0 C to give the mono-benzylated intermediate
- a suitable base e.g. NEt 3 , DIPEA, DCMC
- a suitable solvent such as DMF, NMP or DMPU and preferably at a temperature between 45 and 90 0 C.
- the compound of formula V can be obtained (Scheme 2) by coupling a compound of formula III with a compound of formula IV using standard peptide coupling methods such as PyBOP, in the presence of a suitable base such as NEt 3 , DIPEA or N-methylmorpholine and in a suitable solvent such as DCM, THF or DMF, preferably at a temperature around RT.
- a suitable base such as NEt 3 , DIPEA or N-methylmorpholine
- a suitable solvent such as DCM, THF or DMF
- the resulting intermediate of formula V can then be converted into a compound of formula II wherein W is -NR 3 - by aromatic substitution reaction with an amine of formula HNR 2 R 3 optionally in the presence of a suitable base such as NEt 3 , DIPEA or N-methylmorpholine, the reaction being carried out in a suitable solvent such as DCM, THF, MeCN or DMF and preferably between RT and 70 0 C.
- a suitable base such as NEt 3 , DIPEA or N-methylmorpholine
- the intermediate of formula V can also be converted into a compound of formula II wherein W is -O- by aromatic substitution reaction with an alcohol of formula R 2 OH in the presence of a suitable base such as NaH, the reaction being carried out in a suitable solvent such as MeOH, THF, MeCN or DMF and preferably around RT.
- a suitable base such as NaH
- the intermediate of formula V can furthermore be converted into a compound of formula II wherein W is a bond, using a reagent of formula R 2 -B(OR)2, R being hydrogen or alkyl, using standard conditions for a Suzuki reaction, and preferably using a boronic acid or ester derivative R -B(OR) 2 in the presence of a suitable base such as K3PO4 or K2CO3, in the presence of a suitable palladium catalyst such as tetrakis(triphenylphosphine)palladium or tris(dibenzylideneacetone)dipalladium, optionally in the presence of a suitable ligand such as triphenylphosphine, in a suitable solvent such as dioxane or a toluene/EtOH mixture, and preferably heating between 8O 0 C and 100 0 C.
- a suitable base such as K3PO4 or K2CO3
- a suitable palladium catalyst such as tetrakis(tripheny
- the intermediate of formula V can also be converted into a compound of formula II wherein W is a bond, using a reagent of formula R 2 -SnBu3, using standard conditions for a Stille reaction, and preferably using a tributylstannane derivative R 2 -SnBu3 in the presence of a suitable catalyst such as tetrakis(triphenylphosphine)palladium in a suitable solvent such as toluene, and preferably heating at about 110 0 C.
- a suitable catalyst such as tetrakis(triphenylphosphine)palladium
- the intermediate of formula V can also be converted into a compound of formula II wherein W is a bond, using a magnesium derivative of formula R -MgBr, in the presence of a suitable iron catalyst such as iron(III)acetylacetonate, in a suitable solvent such as THF and at a temperature preferably around RT (see Furstner A. et al. in J. Am. Chem. Soc. (2002), 13856-13863).
- a suitable iron catalyst such as iron(III)acetylacetonate
- the intermediate of formula V can also be converted in a two step procedure into a compound of formula II wherein W is a bond, using a reagent of formula R-C ⁇ CH (R equals RCH 2 CH 2 ), using standard conditions for a Sonogashira reaction, and preferably using an alkyne derivative R-C ⁇ CH in the presence of a suitable base such as NEt 3 , in the presence of a suitable palladium catalyst such as bis-(triphenylphosphine) palladium(II)-dichloride, in the presence of a suitable copper catalyst such as copper(I) iodide, in a suitable solvent such as DMF, and at RT.
- a suitable palladium catalyst such as bis-(triphenylphosphine) palladium(II)-dichloride
- a suitable copper catalyst such as copper(I) iodide
- the obtained intermediate can be converted into a compound of formula II by reducing the triple bond to the single bond in the presence of a suitable catalyst such as Raney Nickel, in a suitable solvent such as MeOH, at a temperature preferably around RT under a hydrogen atmosphere.
- a suitable catalyst such as Raney Nickel
- the compounds of formula II can be prepared as described in Scheme 2a by coupling a compound of formula III with a compound of formula VI using standard peptide coupling methods such as PyBOP, HOBT, EDCI hydrochloride, l ⁇ -dicyclohexylcarbodiimide, HATU, optionally in the presence of a suitable base such as NEt 3 , DIPEA or 7V-methylmorpholine and in a suitable solvent such as DCM, THF or DMF, preferably at a temperature around RT.
- standard peptide coupling methods such as PyBOP, HOBT, EDCI hydrochloride, l ⁇ -dicyclohexylcarbodiimide, HATU, optionally in the presence of a suitable base such as NEt 3 , DIPEA or 7V-methylmorpholine and in a suitable solvent such as DCM, THF or DMF, preferably at a temperature around RT.
- the compounds of formula VIII can be obtained in three steps starting from Boc-3-iodo- L-AIa-OMe or Boc-3-iodo-D-Ala-OMe: an Arbuzov reaction is performed (e.g. using P(OEt) 3 at reflux) followed by a saponification reaction using standard conditions such as NaOH or LiOH in a mixture of water and a suitable organic solvent such as THF, MeOH or EtOH; finally the obtained acid intermediate is coupled with a compound of formula VII using standard peptide coupling methods such as those described for the synthesis of compounds of formula II (see Scheme 2a).
- the compounds of formula III can then be obtained by standard acidic conditions for the removal of a Boc group that are well known to one skilled in the art.
- L-Homoserine or D-homoserine is first protected on the nitrogen atom with a Z group using standard conditions known to one skilled in the art.
- the dicyclohexylamine salt of the obtained molecule is prepared and the methyl ester is formed using MeI in DMF at a temperature around RT.
- the hydroxy function is then substituted by a bromide using standard conditions such as PPI1 3 and CBr 4 , in a suitable solvent such as DCM, preferably between O 0 C and RT.
- the next three steps leading to the compounds of formula IX are performed using conditions such as those already described for the synthesis of the compounds of formula VIII (see Scheme 3).
- the compounds of formula III can then be obtained by cleaving the Z protecting group using standard conditions known to one skilled in the art (e.g. hydrogenation with Pd/C in EtOH).
- the compounds of formula X can be obtained in two steps starting from commercially available ( ⁇ i/)-Z- ⁇ -phosphonoglycine trimethyl ester: a saponification reaction is performed using standard conditions such as NaOH or LiOH in a mixture of water and a suitable organic solvent such as THF, MeOH or EtOH; the obtained acid intermediate is coupled with a compound of formula VII using standard peptide coupling methods such as those described for the synthesis of compounds of formula II (see Scheme 2a).
- the compounds of formula III can then be obtained by standard conditions for the removal of a Z group that are well known to one skilled in the art (e.g. hydrogenation with Pd/C in EtOH).
- Cbz-(L)-Glu-OMe or Cbz-(D)-Glu-OMe can be reduced to the respective alcohol by transforming the acid to a mixed anhydride using, for instance, a chloroformate reagent, in the presence of a suitable base such as 7V-methylmorpholine, in a suitable solvent such as THF, and preferably at about -15°C and subsequent reduction of the mixed anhydride with a suitable reducing agent such as NaBH4 in presence of MeOH, at a temperature around — 15°C.
- the hydroxy function can be substituted by iodide using standard conditions such as imidazole, PPI13 and I 2 , in a suitable solvent such as THF, preferably between 0 0 C and RT.
- the next three steps leading to the compounds of formula XI can be performed using conditions such as those already described for the synthesis of the compounds of formula VIII (see Scheme 3).
- the compounds of formula III can then be obtained by standard conditions for the removal of a Cbz group that are well known to one skilled in the art (e.g. hydrogenation with Pd/C in MeOH).
- the Boc protected (L)-iodophenylalanine derivatives if not commercially available, can be prepared starting from the (L)-iodophenylalanine compounds using standard conditions known to one skilled in the art.
- the acid function of the Boc protected (L)-iodophenylalanine derivatives can first be protected by formation of an ethyl ester using standard conditions known to one skilled in the art.
- the compounds thus obtained can then be converted into the diethyl phosphonate derivatives using diethyl phosphite, in the presence of a suitable base such as NEt 3 , in the presence of a suitable palladium catalyst such as Pd(PPh 3 ) ⁇ in a suitable solvent such as MeCN or toluene, and preferably heating around reflux temperature.
- a suitable base such as NEt 3
- a suitable palladium catalyst such as Pd(PPh 3 ) ⁇
- a suitable solvent such as MeCN or toluene
- the compounds of formula III can be prepared in six steps starting from the commercially available DL-bromo-phenylglycines using conditions such as those already described for the synthesis of the compounds of formula III in Scheme 3d.
- the compounds of formula IV can be prepared using the route described in WO 2006/114774 (see general preparation routes, preparation of the compounds of formula IV, Scheme Aa).
- the compounds of formula VI can be prepared using the reaction shown in Scheme 4 hereafter.
- the intermediate of formula IV can be converted into a compound of formula VI wherein W is a bond, using a reagent of formula R 2 -B(OR)2, R being hydrogen or alkyl, using standard conditions for a Suzuki reaction such as those described for the synthesis of compounds of formula II wherein W is a bond (see Scheme 2).
- the intermediate of formula IV can be converted into a compound of formula VI wherein W is -NR - by aromatic substitution reaction with an amine of formula HNR 2 R 3 using conditions such as those described for the synthesis of compounds of formula II wherein W is -NR - (see Scheme 2).
- the compounds of formula VII can be prepared using the route described in WO 2006/114774 (see general preparation routes, preparation of the compounds of formula V, Schemes 5 and 5 a).
- the eluent flow rate was 4.5 ml/min and the characteristics of the eluting mixture proportion in function of the time t from start of the elution are summarized in the table below (a linear gradient being used between two consecutive time points):
- the eluent flow rate was 3 ml/min and the characteristics of the eluting mixture proportion in function of the time t from start of the elution are summarized in the table below (a linear gradient being used between two consecutive time points):
- a Phenomenex ® column (Gemini 1Ou Cl 8 HOA Ax 50x21.2 mm) or a X-Terra® column (Prep MS Cl 8 OBDTM 1Ou 30x75 mm) was used.
- the eluent flow rate was 50 mL/min for the Phenomenex ® column and 100 mL/min for the X-Terra ® column.
- the characteristics of the eluting mixture proportion in function of the time t from start of the elution are summarized in the tables below (a linear gradient being used between two consecutive time points):
- the purifications by CC have been performed using silica gel unless otherwise specified.
- the reverse phase used is ISOLUTE® Cl 8 from Biotage.
- Example 1 4-((i?)-2- ⁇ [6-((S)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidiiie- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid ethyl ester:
- HOBT hydrate (98 mg) and EDCI hydrochloride (123 mg) were added to a solution of intermediate 1.2 (200 mg) and DIPEA (0.42 mL) in THF/DCM (0.6 mL / 2.4 mL). After stirring at RT for 10 min, 1 -ethoxycarbonylpiperazine (97 mg) was added and the stirring was continued overnight at RT. DCM and an aq. NaHCO 3 solution were added to the mixture and the phases were separated. The aq. phase was extracted with DCM and the combined org. phases were washed with a NaCl solution, dried (Na 2 SO ⁇ and evaporated off.
- Example 3 4-((5)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid ethyl ester:
- Example 4 4-((5)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid ethyl ester:
- Example 8 4-((5)-2- ⁇ [6-(4-methyl-pyrazol-l-yl)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid butyl ester: 8.1. 4-((S)-4-(diethoxy-phosphoryl)-2- ⁇ [6-(4-methyl-pyrazol-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -butyryl)-piperazine-l-carboxylic acid butyl ester:
- Example 10 4- ⁇ (5)-2-[(2-phenyl-6-pyrrolidin-l-yl-pyrimidine-4-carbonyl)-amino]- 4-phosphono-butyryl ⁇ -piperazine-l-carboxylic acid butyl ester: 10.1. 4- ⁇ (S)-4-(diethoxy-phosphoryl)-2-[(2-phenyl-6-pyrrolidin-l-yl-pyrimidine-4-carbonyl)- amino] -butyrylj-piperazine-1-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1, step 1.10, intermediate 10.1 replacing intermediate 1.9.
- the crude was purified by preparative LC-MS (I).
- Example 11 4- ⁇ (5)-2- [(6-isopropylamino-2-phenyl-pyrimidine-4-carbonyl)-amino] - 4-phosphono-butyryl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 14 4- ⁇ (i?)-2-[(6-methylamino-2-phenyl-pyrimidine-4-carbonyl)-amino]- 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 16 4- ⁇ (i?)-2-[(6-ethylamino-2-phenyl-pyrimidine-4-carbonyl)-amino]- 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 17.1 replacing intermediate 1.9.
- the crude was purified by CC (reverse phase, eluent A: water/TFA 100/1; eluent B: MeCN/TFA 100/1; gradient: 5% B/l CV; 5% to 70% B/20 CV; 70% B/4 CV).
- Example 18 4-((5)-2- ⁇ [2-(4-fluoro-phenyl)-6-((5)-3-methoxy-pyrrolidin-l-yl)- pyrimidine-4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared in 4 steps from intermediate 18.1 using methods analog to those described in WO 2006/114774 (see Example 1, step 1.3 and Example 24, steps 24.1, 24.2 and 24.3).
- This compound was prepared using a method analogous to that of Example 1, step 1.8, intermediate 18.2 replacing 6-chloro-2-phenyl-pyrimidine-4-carboxylic acid. The product was however not purified.
- Example 19 4-((5)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-/j-tolyl-pyrimidine- 4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid butyl ester:
- ⁇ -chloro ⁇ -p-tolyl-pyrimidine ⁇ -carboxylic acid This compound was prepared in 4 steps from 4-methyl-benzamidine using methods analog to those described in WO 2006/114774 (see Example 1, step 1.3, Example 24, steps 24.1, 24.2 and 24.3).
- LC-MS (A): t R 0.93 min; [M+H] + : 249.28.
- This compound was prepared using a method analogous to that of Example 1, step 1.10, intermediate 19.3 replacing intermediate 1.9.
- the crude was purified by preparative LC-MS (II).
- Example 20 4-((5)-2- ⁇ [2-(2-fluoro-phenyl)-6-((5)-3-methoxy-pyrrolidin-l-yl)- pyrimidine ⁇ -carbonylj-aminoj ⁇ -phosphono-butyry ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 22 4- ⁇ (i?)-2-[(6-methoxy-2-phenyl-pyrimidine-4-carbonyl)-amino]- 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 23 4- ⁇ (R)-2- [(6-methyl-2-phenyl-pyrimidine-4-carbonyl)-amino] - 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 24 4- ⁇ (R)-2- [( ⁇ -cyclopropylamino ⁇ -phenyl-pyrimidine ⁇ -carbony ⁇ -amino] - 3-phosphono-propionylJ-piperazine-l-carboxylic acid butyl ester:
- Example 25 4- ⁇ (i?)-2-[(2-phenyl-6-phenylamino-pyrimidine-4-carbonyl)-amino]- 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1, step 1.8, benzylamine replacing intermediate 1.7, intermediate 14.1 replacing 6-chloro-2-phenyl- pyrimidine-4-carboxylic acid and heating at 70 0 C instead of 60 0 C.
- the product was however not purified.
- Example 27 4-[(i?)-2-( ⁇ 2-phenyl-6-[(i?)-(tetrahydro-furan-3-yl)amino]-pyrimidiiie- 4-carbonyl ⁇ -amino)-3-phosphono-propionyl]-piperazine-l-carboxylic acid butyl ester:
- Example 29 4- [(R)-2-( ⁇ 6- [(2-methoxy-ethyl)-methyl-amino] -2-phenyl-pyrimidine- 4-carbonyl ⁇ -amino)-3-phosphono-propionyl]-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1, step 1.10, intermediate 29.1 replacing intermediate 1.9.
- the crude was purified by preparative LC-MS (II).
- Example 30 4-((i?)-2- ⁇ [6-(2-ethoxycarbonyl-ethylamino)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1, step 1.10, intermediate 30.1 replacing intermediate 1.9.
- the crude was purified by preparative LC-MS (II).
- Example 31 4-((i?)-2- ⁇ [6-(2-carboxy-ethylamino)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 32 4- ⁇ (R)-2- [(2,6-diphenyl-pyrimidine-4-carbonyl)-amino] -3-phosphono- propionylj-piperaziiie-l-carboxylic acid butyl ester:
- Example 33 4- ⁇ (i?)-2-[(2-phenyl-6-thiophen-3-yl-pyrimidine-4-carbonyl)-amiiio]- 3-phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 34 4-((i?)-2- ⁇ [6-(4-methoxy-phenyl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ - 3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 35 4- ⁇ (R)-2- [(6-cyclopropyl-2-phenyl-pyrimidine-4-carbonyl)-amino] - 3-phosphono-propionylJ-piperazine-l-carboxylic acid butyl ester:
- Example 37 4-[(i?)-2-( ⁇ 2-phenyl-6-[(S)-(tetrahydro-furan-3-yl)oxy]-pyrimidiiie- 4-carbonyl ⁇ -amino)-3-phosphono-propionyl]-piperazine-l-carboxylic acid butyl ester:
- Example 38 4-((R)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-2-methyl-piperazine-l-carboxylic acid ethyl ester:
- This compound was prepared using a method analogous to that of Example 32, step 32.2, intermediate 38.3 replacing intermediate 32.1 and using 4 M HCl in dioxane instead of 3 M HCl in EA.
- Example 39 4-((R)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid ethyl ester:
- Example 40 4-((R)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid butyl ester:
- Example 41 4-((i?)-2- ⁇ [6-((7 1 S',25)-2-methoxymethyl-cyclopropyl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 42 4-((R)-2- ⁇ [6-((7S,25)-2-hydroxymethyl-cyclopropyl)-2-phenyl-pyrimidine- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 43 4-((i?)-2- ⁇ [6-(2-hydroxy-ethylamino)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 44 4-((i?)-2- ⁇ [6-(2-hydroxymethyl-piperidin-l-yl)-2-phenyl-pyrimidiiie- 4-carbonyl]-amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 45 4-((i?)-2- ⁇ [6-(3-methoxy-propyl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ - 3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 46 4-((i?)-2- ⁇ [6-(3-hydroxy-butyl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ - 3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 47 4-((5)-2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-(3-trifluoromethyl-phenyl)- pyrimidine-4-carbonyl]-amino ⁇ -4-phosphono-butyryl)-piperazine-l-carboxylic acid butyl ester:
- Example 51 4-((R)-3-[A/s r -(2,2-dimethyl-propionyloxymethoxy)-phosphoryl]- 2- ⁇ [6-((S)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ - propionyl)-piperazine-l-carboxylic acid butyl ester:
- Example 52 4-((i?)-3- ⁇ Z>/s-[l-(2,2-dimethyl-propionyloxy)-ethoxy]-phosphoryl ⁇ - 2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ - propiony ⁇ -piperazine-l-carboxylic acid butyl ester: To a solution of the compound of Example 2 (200 mg) in anh. DMPU (0.586 mL) was added TEA (0.135 ml) and the mixture was stirred for 10 min under argon. 1-chloroethyl pivalate (0.516 mL; prepared as described in Synth. Commun.
- Example 53 4-((R)-3-[Z>/s-(l-isobutyryloxy-ethoxy)-phosphoryl]-2- ⁇ [6-((5)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine- 1-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 52, 1-chloroethyl isobutyrate (prepared as described in Synth. Commun. (1995), 25(18), 2739-2749) replacing 1-chloroethyl pivalate.
- Example 54 4-((i?)-3-[Z>/s-(l-propionyloxy-ethoxy)-phosphoryl]-2- ⁇ [6-((5)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine- 1-carboxylic acid butyl ester:
- Example 56 4-(2- ⁇ [6-((5)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -2-phosphono-acetyl)-piperazine-l-carboxylic acid butyl ester:
- Example 58 4-((S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonylJ-aminoJ-S-phosphono-peiitanoy ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 58.7 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase, water/MeCN 1/0 to 0/1).
- Example 59 4-[(S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonyl]-amino ⁇ -3-(4-phosphono-phenyl)-propionyl]-piperazine-l-carboxylic acid ethyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 59.3 replacing intermediate 56.1, 1 -ethoxycarbonylpiperazine replacing intermediate 2.2 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (First purification: Hept/EA 1/0 to 3/1; followed by: eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B; second purification: eluant A: EA, eluant B: EA/MeOH 40/1, 0 to 100% B).
- LC-MS (A): t R 0.93 min; [M+H] + : 542.01. 59.5. 4- ⁇ (S)-2-Amino-3-[4-(diethoxy-phosphoryl)-phenyl]-propionyl ⁇ -piperazine-l-carboxylic acid ethyl ester hydrochloride salt:
- Example 60 4-[(S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonyl]-amino ⁇ -3-(4-phosphono-phenyl)-propionyl]-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 59.3 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (First purification: eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 40% B; second purification: eluant A: EA, eluant B: EA/MeOH 40/1, 0 to 100% B).
- LC-MS (A): t R 1.00 min; [M+H] + : 569.98. 60.2.
- Example 61 4- [(S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonyl]-amino ⁇ -3-(4-phosphonomethyl-phenyl)-propionyl]-piperazine-l-carboxylic acid ethyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.3, Fmoc- p(CH2-PO3Et2)-L-Phe-OH replacing intermediate 1.2.
- the Fmoc group was cleaved during the reaction.
- the compound was purified by CC (eluant A: EA/NEt 3 100/1, eluant B: EA/MeOH/NEt 3 50/50/1, 0 to 100% B, followed by elution with MeOH) to afford 448 mg of the desired compound.
- LC-MS (A): t R 0.71 min; [M+H] + : 456.08.
- Example 62 4-[(S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonyl]-amino ⁇ -3-(4-phosphonomethyl-phenyl)-propionyl]-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.3, Fmoc- p(CH 2 -PO 3 Et 2 )-L-Phe-OH replacing intermediate 1.2 and intermediate 2.2 replacing 1-ethoxy- carbonylpiperazine.
- the Fmoc group was cleaved during the reaction.
- the compound was purified by CC (eluant A: EA/NEt 3 100/1, eluant B: EA/MeOH/NEt 3 50/50/1, 0 to 100% B) to afford 448 mg of the desired compound.
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 62.1 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (eluant A: EA, eluant B: EA/MeOH 9/1, first purification: 0 to 100% B; second purification: 20 to 100% B).
- LC-MS (A): t R 1.12 min; [M+H] + : 765.02.
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 62.2 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O + 1% TFA; eluant B: MeCN + 1% TFA; gradient: 5 to 90% B).
- LC-MS (A): t R 0.97 min; [M+H] + : 709.15.
- Example 63 4-((R)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonylJ-aminoJ-S-phosphono-peiitanoy ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 63.4 replacing intermediate 56.1.
- the compound was purified by CC (Hept/EA 2/8, then EA/MeOH 10/1).
- Example 64 4- ⁇ (R)-2-[(6-Isopropyl-2-phenyl-pyrimidine-4-carbonyl)-amino]-3- phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 64.1 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O + 1% TFA; eluant B: MeCN + 1% TFA; gradient: 5 to 80% B).
- LC-MS (A): t R 0.95 min; [M+H] + : 561.98.
- Example 65 4-((R)-2- ⁇ [6-(3-Methoxymethyl-azetidin-l-yl)-2-phenyl-pyrimidine-4- carbonylJ-aminoJ-S-phosphono-propiony ⁇ -piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 2 step 2.2, a mixture of MeOH/lMHCl 1/0.1 replacing EtOH.
- Example 66 4- ⁇ (R)-2-[(6-Cyclopentyloxy-2-phenyl-pyrimidine-4-carbonyl)-amino]-3- phosphono-propionylj-piperazine-l-carboxylic acid ethyl ester:
- Example 67 4- [(S)-2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4- carbonyl]-amino ⁇ -3-(4-phosphono-phenyl)-propionyl]-piperazine-l-carboxylic acid ethyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 67.3 replacing intermediate 56.1, 1 -ethoxycarbonylpiperazine replacing intermediate 2.2 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (first purification: eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B; second purification: eluant A: Hept, eluant B: EA, 50 to 100% B).
- LC-MS (A): t R 0.94 min; [M+H] + : 542.38.
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 67.6 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O + 1% TFA; eluant B: MeCN + 1% TFA; gradient: 5 to 80% B).
- LC-MS (A): t R 0.90 min; [M+H] + : 667.64.
- Example 68 4-[2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -2-(4-phosphono-phenyl)-acetyl]-piperazine-l-carboxylic acid ethyl ester:
- This compound was prepared using a method analogous to that of Example 59 step 59.1, intermediate 68.1 replacing Boc-Phe(4-I)-OH.
- the compound was purified by CC (Hept/EA, 1/0 to 0/1).
- This compound was prepared using a method analogous to that of Example 56 step 56.2, 1- ethoxycarbonylpiperazine replacing intermediate 2.2, intermediate 68.4 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the crude was purified by CC (eluant A: EA, eluant B: EA/MeOH 40/1, 0 to 20% B).
- LC-MS (A): t R 0.95 min; [M+H] + : 528.64.
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 68.6 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B).
- LC-MS (A): t R 1.08 min; [M+H] + : 709.74.
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 69.2 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B).
- LC-MS (A): t R 1.13 min; [M+H] + : 737.78.
- This compound was prepared using a method analogous to that of Example 59 step 59.1, intermediate 70.1 replacing Boc-Phe(4-I)-OH.
- the compound was purified by CC (Hept/EA, 1/0 to 1/1).
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 70.6 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B).
- LC-MS (A): t R 1.09 min; [M+H] + : 709.80.
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 70.7 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O; eluant B: MeCN; gradient: 5 to 80% B).
- LC-MS (A): t R 0.90 min; [M+H] + : 653.24.
- Example 71 4-[2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -2-(3-phosphono-phenyl)-acetyl]-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 71.2 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (First CC: eluant A: EA, eluant B: EA/MeOH 9/1, 0 to 100% B; second CC: reverse phase, eluant A: H 2 O; eluant B: MeCN; gradient: 5 to 90% B).
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 71.3 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O; eluant B: MeCN; gradient: 5 to 80% B).
- LC-MS (A): t R 0.96 min; [M+H] + : 681.22.
- Example 72 4-[2- ⁇ [6-((S)-3-Methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]- amino ⁇ -2-(2-phosphono-phenyl)-acetyl]-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 56 step 56.2, intermediate 72.6 replacing intermediate 2.2, intermediate 1.8 replacing intermediate 56.1 and using DCM/THF 4/1 instead of DCM.
- the compound was purified by CC (eluant A: EA, eluant B: EA/MeOH 100/1, 0 to 100% B).
- LC-MS (A): tR. 1.11 min; [M+H] + : 737.81. 72.8.
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 72.7 replacing intermediate 1.9.
- the compound was purified by CC (reverse phase; eluant A: H 2 O; eluant B: MeCN; gradient: 5 to 80% B).
- LC-MS (A): t R 1.00 min; [M+H] + : 681.22.
- Example 73 4-((R)-2- ⁇ [6-(4-Methyl-piperazin-l-yl)-2-phenyl-pyrimidine-4-carboiiyl]- amino ⁇ -3-phosphono-propionyl)-piperazine-l-carboxylic acid butyl ester:
- This compound was prepared using a method analogous to that of Example 1 step 1.10, intermediate 73.1 replacing intermediate 1.9.
- the crude was purified by CC (reverse phase; eluant A: H 2 O; eluant B: MeCN; gradient: 5 to 80% B) followed by preparative TLC (EA/MeOH 1/1 then EA/MeOH 1/2).
- Example 74 4- ⁇ (R)-2- [(6-Morpholin-4-yl-2-phenyl-pyrimidine-4-carbonyl)-amino] -3- phosphono-propionyl ⁇ -piperazine-l-carboxylic acid butyl ester:
- Example 75 N,N'-Bis-(ethoxycarbonylmethyl)-3- ⁇ (S)-[6-((S)-3-methoxy-pyrrolidin-l- yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -4-oxo-4-(4-butoxy-carbonyl-piperaziii-l-yl)- butyl-phosphonic acid diamide:
- Example 76 4-((R)-3-(Bis-acetoxymethoxy-phosphoryl)-2- ⁇ [6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine-l- carboxylic acid butyl ester:
- Example 77 4-((R)-3-(Bis-propionyloxymethoxy-phosphoryl)-2- ⁇ [6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine-l- carboxylic acid butyl ester:
- Example 78 4-((R)-3-(Bis-butyryloxymethoxy-phosphoryl)-2- ⁇ [6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine-l- carboxylic acid butyl ester:
- Example 79 N,N'-Bis-(ethoxycarbonylmethyl)-2- ⁇ (R)-[6-((S)-3-methoxy-pyrrolidin-l- yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl-piperazin-l-yl)- propyl-phosphonic acid diamide:
- Example 80 N,N'-Bis-((S)-l-ethoxycarbonylethyl)-2- ⁇ (R)-[6-((S)-3-methoxy-pyrrolidin- l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl-piperazin-l- yl)-propyl-phosphonic acid diamide:
- Example 81 N,N'-Bis-(methoxycarbonylmethyl)-2- ⁇ (R)-[6-((S)-3-methoxy-pyrrolidin-l- yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl-piperaziii-l-yl)- propyl-phosphonic acid diamide: This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and glycine methyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- LC-MS (A): t R 0.98 min; [M+H] + : 760.92.
- Example 82 N,N'-Bis-((S)-l-methoxycarbonyl-2-methyl-propyl)-2- ⁇ (R)-[6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy- carbonyl-piperazin-l-yl)-propyl-phosphoiiic acid diamide:
- Example 83 N,N'-Bis-(tert-butyloxycarbonylmethyl)-2- ⁇ (R)-[6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl- piperazin-l-yl)-propyl-phosphonic acid diamide:
- Example 84 N,N'-Bis-((S)-l-methoxycarbonylpropyl)-2- ⁇ (R)-[6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl- piperazin-l-yl)-propyl-phosphonic acid diamide: This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and 2-aminobutyric acid methyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- LC-MS (A): t R 1.07 min; [M+H] + : 817.05.
- Example 85 N,N'-Bis-((S)-l-methoxycarbonyl-2,2-dimethyl-propyl)-2- ⁇ (R)-[6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy- carbonyl-piperazin-l-yl)-propyl-phosphonic acid diamide:
- This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and tert-leucine methyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- Example 86 N,N'-Bis-((S)-l-tert-butyloxycarbonyl-ethyl)-2- ⁇ (R)-[6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl- piperazin-l-yl)-propyl-phosphonic acid diamide: This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and alanine tert-butyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- LC-MS (A): t R 1.16 min; [M+H] + : 873.11.
- Example 87 N,N'-Bis-((S)-l-methoxycarbonyl-2-phenyl-ethyl)-2- ⁇ (R)-[6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy- carbonyl-piperazin-l-yl)-propyl-phosphoiiic acid diamide:
- Example 88 N,N'-Bis-((S)-l-methoxycarbonyl-l-phenyl-methyl)-2- ⁇ (R)-[6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy- carbonyl-piperazin-l-yl)-propyl-phosphonic acid diamide:
- Example 90 N,N'-Bis-(propyloxycarbonyl-methyl)-2- ⁇ (R)-[6-((S)-3-methoxy-pyrrolidin- l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl-piperazin-l- yl)-propyl-phosphonic acid diamide:
- This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and glycine propyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- Example 91 N,N'-Bis-(isopropyloxycarbonyl-methyl)-2- ⁇ (R)-[6-((S)-3-methoxy- pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -3-oxo-3-(4-butoxy-carbonyl- piperazin-l-yl)-propyl-phosphonic acid diamide: This compound was prepared using a method analogous to that of Example 75, intermediate 2.6 replacing intermediate 5.4 and glycine isopropyl ester hydrochloride replacing glycine ethyl ester hydrochloride.
- Example 93 4-((R)-3-[Bis-(methoxycarbonyloxy-methoxy)-phosphoryl]-2- ⁇ [6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
- Example 94 4-((R)-3-[Bis-(ethoxycarbonyloxymethoxy)-phosphoryl]-2- ⁇ [6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
- Example 96 4-((R)-3-[Bis-(tert-butoxycarbonyloxy-methoxy)-phosphoryl]-2- ⁇ [6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
- Example 97 4-((R)-3-[Bis-(l-ethyloxycarbonyloxy-ethoxy)-phosphoryl]-2- ⁇ [6-((S)-3- methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
- This compound was prepared using a method analogous to that of Example 93, 1-chloroethyl ethyl carbonate replacing chloromethyl methyl carbonate and was isolated as mixture of diastereoisomers.
- Example 98 4-((R)-3-[Bis-(l-isopropyloxycarbonyloxy-ethoxy)-phosphoryl]-2- ⁇ [6-((S)- 3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
- This compound was prepared using a method analogous to that of Example 93, 1-chloroethyl isopropyl carbonate replacing chloromethyl methyl carbonate and was isolated as mixture of diastereoisomers.
- LC-MS (A): t R 1.18 min; [M+H] + : 879.01.
- Example 100 4-((R)-3-(Diphenoxy-phosphoryl)-2- ⁇ [6-((S)-3-methoxy-pyrrolidin-l-yl)- 2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)-piperazine-l-carboxylic acid butyl ester
- Example 101 4-((R)-3-[Bis-(5-methyl-2-oxo-[l,3]dioxol-4-ylmethoxy)-phosphoryl]-2- ⁇ [6-((S)-3-methoxy-pyrrolidin-l-yl)-2-phenyl-pyrimidine-4-carbonyl]-amino ⁇ -propionyl)- piperazine-1-carboxylic acid butyl ester
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EP08855100A EP2225253B1 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
ES08855100T ES2388958T3 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivatives and their use as a P2Y12 receptor antagonist |
MX2010005519A MX2010005519A (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists. |
US12/745,358 US8518912B2 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as P2Y12 receptor antagonists |
KR1020107012062A KR101178319B1 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
AU2008331163A AU2008331163B2 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as P2Y12 receptor antagonists |
CN200880116983.8A CN101868469B (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and application thereof as P2Y12 receptor antagonists |
JP2010535498A JP4729133B2 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivatives and their use as P2Y12 receptor antagonists |
DK08855100.7T DK2225253T3 (en) | 2007-11-29 | 2008-11-28 | PHOSPHONIC ACID DERIVATIVES AND THEIR USE AS P2Y12 RECEPTOR ANTAGONISTS |
CA2706475A CA2706475C (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
RU2010126048/04A RU2483072C2 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivatives and use thereof as p2y12 receptor antagonists |
NZ586445A NZ586445A (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
PL08855100T PL2225253T3 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
BRPI0819696A BRPI0819696B1 (en) | 2007-11-29 | 2008-11-28 | 2-phenyl pyrimidine derivative compounds, pharmaceutical composition and use of a compound |
SI200830722T SI2225253T1 (en) | 2007-11-29 | 2008-11-28 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
IL205947A IL205947A (en) | 2007-11-29 | 2010-05-25 | Phosphonic acid derivatives and their use as p2y12 receptor antagonists |
MA32897A MA31983B1 (en) | 2007-11-29 | 2010-06-08 | Phosphonic acid derivatives and their use as antagonists of the p2y12 receptor |
HK11102247.4A HK1148287A1 (en) | 2007-11-29 | 2011-03-07 | Phosphonic acid derivates and their use as p2y12 receptor antagonists |
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