HCID 10362721, compound → HCID 10359004, compound

HRID 1271859Notes

Reaction equation

HRID 1271859 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][O:29][CH3:30])=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16])(C)(C)C.NC1C=CC=CC=1NC(C1SC2C=CC(OCCOCCOC)=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][O:29][CH3:30])=[CH:24][CH:23]=[CH:22][C:20]=2[CH:21]=1)=[O:16]

Participants

3

Reactant 2

HCID 10362721HCID 10362721, compoundHCID 69489877HCID 69489877, compound

Product 1

HCID 10359004HCID 10359004, compound

Procedure

was prepared from (2-{[7-(2-Methoxy-ethoxy)-benzofuran-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester (34) in an analogous manner to that described for the preparation of (27) example 11, step 2; exact MW [M+H] calc'd: 327.13; MW found [M+H]: 327.0.

Sources & evidence

ORD record
ord-f475a6018e4340bc8527c9982df7a475
Source dataset
uspto-grants-2007_04
Patent number
US07208491B2

Reaction notes

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