HCID 44217798, compound → HCID 67108801, compound

HRID 2074531Notes

Reaction equation

HRID 2074531 reaction equation
C(N1C2C(=CC=CC=2)C(COC(C)(C)CO)=N1)C1C=CC=CC=1.[CH3:24][O:25][C:26]1[CH:49]=[CH:48][C:29]([CH2:30][N:31]2[C:39]3[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=3)[C:33]([CH2:40][O:41][C:42]([CH3:47])([CH3:46])[C:43](O)=[O:44])=[N:32]2)=[CH:28][CH:27]=1>>[CH3:24][O:25][C:26]1[CH:27]=[CH:28][C:29]([CH2:30][N:31]2[C:39]3[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=3)[C:33]([CH2:40][O:41][C:42]([CH3:47])([CH3:46])[CH2:43][OH:44])=[N:32]2)=[CH:48][CH:49]=1

Participants

3

Procedure

The product was obtained with the method described for the preparation of compound 39a, using 2-{[1-(4-methoxybenzyl)-1H-indazol-3-yl]methoxy}-2-methylpropanoic acid as starting material.

Workup

  1. customThe product was obtained with the method

Sources & evidence

ORD record
ord-5f3ae6e695154382b3cf98cc91a788ba
Source dataset
uspto-grants-2011_04
Patent number
US07919518B2

Reaction notes

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