Methyl Acrylate → HCID 68704344, compound

HRID 2242873Notes

Reaction equation

HRID 2242873 reaction equation
[Cl:1][C:2]1[N:3]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH2:18][C@H:19]3[CH2:23][CH2:22][CH2:21][NH:20]3)=[CH:13][CH:12]=2)[N:4]=[C:5]2[C:10]=1[CH:9]=[CH:8][CH:7]=[CH:6]2.[C:24]([O:28][CH3:29])(=[O:27])[CH:25]=[CH2:26]>>[CH3:29][O:28][C:24](=[O:27])[CH2:25][CH2:26][N:20]1[CH2:21][CH2:22][CH2:23][C@@H:19]1[CH2:18][O:17][C:14]1[CH:13]=[CH:12][C:11]([N:3]2[C:2]([Cl:1])=[C:10]3[C:5]([CH:6]=[CH:7][CH:8]=[CH:9]3)=[N:4]2)=[CH:16][CH:15]=1

Participants

3

Procedure

The title compound was prepared from product from 3-chloro-2-[4-((R)-1-pyrrolidin-2-ylmethoxy)-phenyl]-2H-indazole (0.4 g, 1.1 mmol) and methyl acrylate (0.25 g, 3.4 mmol) using the procedure of step 5 of the Example 4 to provide the title compound (0.37 g, 79%).

Sources & evidence

ORD record
ord-42b4313e30dd48428171de0fdeeaa078
Source dataset
uspto-grants-2010_03
Patent number
US07674802B2

Reaction notes

Loading…