HCID 10427468, compound → HCID 69489669, compound

HRID 1271867Notes

Reaction equation

HRID 1271867 reaction equation
C([O:5][C:6](=[O:35])[CH2:7][O:8][C:9]1[C:17]2[O:16][C:15]([C:18](=[O:34])[NH:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[NH:26]C(OC(C)(C)C)=O)=[CH:14][C:13]=2[CH:12]=[CH:11][CH:10]=1)(C)(C)C.NC1C=CC=CC=1NC(C1SC2C=CC(OCC(O)=O)=CC=2C=1)=O>>[NH2:26][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=1[NH:19][C:18]([C:15]1[O:16][C:17]2[C:9]([O:8][CH2:7][C:6]([OH:35])=[O:5])=[CH:10][CH:11]=[CH:12][C:13]=2[CH:14]=1)=[O:34]

Participants

3

Reactant 2

HCID 10427468HCID 10427468, compoundHCID 69489688HCID 69489688, compound

Product 1

HCID 69489669HCID 69489669, compound

Procedure

was prepared from [2-(2-tert-Butoxycarbonylamino-phenylcarbamoyl)-benzofuran-7-yloxy]-acetic acid tert-butyl ester (48) in an analogous manner to that described for the preparation of (45) example 19, step 2; mp.: 208–210° C.

Sources & evidence

ORD record
ord-1f8338cefb0e48f6a0917a27e165418d
Source dataset
uspto-grants-2007_04
Patent number
US07208491B2

Reaction notes

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