HCID 44217327, compound → HCID 86648330, compound

HRID 2074533Notes

Reaction equation

HRID 2074533 reaction equation
C(N1C2C(=CC=CC=2)C(COC(C)(C)C([NH:23][OH:24])=O)=N1)(=O)C1C=CC=CC=1.[CH2:27]([N:34]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[C:36]([CH2:43][O:44][CH2:45][CH2:46][O:47][C:48]([CH3:53])([CH3:52])[C:49](O)=[O:50])=[N:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH2:27]([N:34]1[C:42]2[C:37](=[CH:38][CH:39]=[CH:40][CH:41]=2)[C:36]([CH2:43][O:44][CH2:45][CH2:46][O:47][C:48]([CH3:53])([CH3:52])[C:49]([NH:23][OH:24])=[O:50])=[N:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1

Participants

3

Procedure

The product was obtained with the method described for the preparation of compound 34e), using 2-{2-[(1-benzyl-1H-indazol-3-yl)methoxy]ethoxy}-2-methylpropanoic acid as starting material.

Workup

  1. customThe product was obtained with the method

Sources & evidence

ORD record
ord-99e824eb4c4c4dcc8ae40df4cd9664db
Source dataset
uspto-grants-2011_04
Patent number
US07919518B2

Reaction notes

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