An 17 Reaktionen beteiligt

1096333

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57620

(S)-2-{4′-[(4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

CCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12

Reaction #57624

(S)-2-{4′-[(4-ethoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

CCCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12

Reaction #57628

(S)-2-{4′-[(3-methyl-4-propoxy-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC(C)C)c4c3C)cc2)cc1)C(C)C

Reaction #57632

(S)-2-{4′-[(4-Isopropoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5ccccc5)c4c3C)cc2)cc1)C(C)C

Reaction #57636

(S)-3-methyl-2-{4′-[(3-methyl-4-phenyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester

Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5cccc([N+](=O)[O-])c5)c4c3C)cc2)cc1)C(C)C

Reaction #57640

(S)-3-methyl-2-(4′-{[3-methyl-4-(3-nitro-phenyl)-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-butyric acid methyl ester

Ausbeute 18.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5cccnc5)c4c3C)cc2)cc1)C(C)C

Reaction #57643

(S)-3-methyl-2-{4′-[(3-methyl-4-pyridin-3-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester

Ausbeute 39.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5ccncc5)c4c3C)cc2)cc1)C(C)C

Reaction #57646

(S)-3-methyl-2-{4′-[(3-methyl-4-pyridin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester

Ausbeute 82.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5ccoc5)c4c3C)cc2)cc1)C(C)C

Reaction #57650

(S)-2-{4′-[(4-furan-3-yl-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(N5CCOCC5)c4c3C)cc2)cc1)C(C)C

Reaction #57654

(S)-3-methyl-2-{4′-[(3-methyl-4-morpholin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester

Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(Cl)c(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57664

(S)-2-{4′-[(5-chloro-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(Br)c(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57674

(S)-2-{4′-[(5-bromo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(I)c(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57683

(S)-2-{4′-[(5-iodo-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 47.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(C(C)=O)c(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57686

(S)-2-{4′-[(5-acetyl-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

C=C(Cl)c1ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c2c1OC

Reaction #57690

(S)-2-(4′-{[5-(1-chloro-vinyl)-4-methoxy-3-methyl-benzofuran-2-carbonyl]-amino}-biphenyl-4-sulfonylamino)-3-methyl-butyric acid methyl ester

Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(C(C)=O)c(O)c4c3C)cc2)cc1)C(C)C

Reaction #57693

(S)-2-{4′-[(5-acetyl-4-hydroxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 11.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4ccc(C#N)c(OC)c4c3C)cc2)cc1)C(C)C

Reaction #57699

(S)-2-{4′-[(5-cyano-4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester

Ausbeute 32.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09