HCID 10248891, compound → HCID 10247869, compound

Reaction equation

C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15]([C:17]1[O:18][C:19]2[C:25]([O:26][CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][N:29]=3)=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16])(C)(C)C.NC1C=CC=CC=1NC(C1SC2C=CC(OCC3C=CC=CN=3)=CC=2C=1)=O>>[NH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15]([C:17]1[O:18][C:19]2[C:25]([O:26][CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][N:29]=3)=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16]

Participants

Reactant 2

HCID 10248891HCID 10248891, compound

HCID 69489954HCID 69489954, compound

Product 1

HCID 10247869HCID 10247869, compound

Procedure

was prepared from (2-{[7-(Pyridin-2-ylmethoxy)-benzofuran-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester (54) in an analogous manner to that described for the preparation of (51) example 22, step 2; mp.: 105–135° C.

Sources & evidence

ORD record: ord-a16964828813430885e57965a0697089
Source dataset: uspto-grants-2007_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07208491B2

Reaction notes

Loading…