HCID 10089559, compound → HCID 10068287, compound

HRID 1271853Notes

Reaction equation

HRID 1271853 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][CH2:28][N:29]3[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]3)=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16])(C)(C)C.NC1C=CC=CC=1NC(C1SC2C=CC(OCCN(C)C)=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][CH2:28][N:29]3[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34]3)=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16]

Participants

3

Reactant 2

HCID 10089559HCID 10089559, compoundHCID 69489920HCID 69489920, compound

Product 1

HCID 10068287HCID 10068287, compound

Procedure

was prepared from (2-{[7-(2-Piperidin-1-yl-ethoxy)-benzofuran-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester (22) in an analogous manner to that described for the preparation of (1) example 1, step 5; white solid; exact MW [M+H] calc'd: 380.20; MW found [M+H]: 380.2.

Sources & evidence

ORD record
ord-f5dbd0642c0e4bb6b09643a8b08dbd3c
Source dataset
uspto-grants-2007_04
Patent number
US07208491B2

Reaction notes

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