Propionate ion → HCID 18947609, compound

HRID 1769352Notes

Reaction equation

HRID 1769352 reaction equation
[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[C:11]([OH:16])[CH:12]=[CH:13][CH:14]=3)[CH:9]=[C:8]2[CH2:17][C:18]([CH3:24])([CH3:23])[C:19]([O:21]C)=[O:20])=[CH:4][CH:3]=1.[C:27]([O-])(=O)[CH2:28][CH3:29]>>[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[C:11]([O:16][CH2:29][C:28]4[CH:27]=[CH:9][C:10]5[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=5)[N:7]=4)[CH:12]=[CH:13][CH:14]=3)[CH:9]=[C:8]2[CH2:17][C:18]([CH3:24])([CH3:23])[C:19]([OH:21])=[O:20])=[CH:4][CH:3]=1

Participants

3

Procedure

The title product was prepared according to conditions described in Steps D and E of Example 1 substituting methyl 3-[N-(p-chlorobenzyl)-4-hydroxy indol-2-yl]-2,2-dimethylpropanoate for the propanoate in Example 1 (Step D), m.p. 158°-160° C. Anal. C, H, N: Calc. C 72.20; H 5.45; N 5.61 Found C 72.25; H 5.60; N 5.75.

Sources & evidence

ORD record
ord-c788bac19af7498b9690d1f36df1f21c
Source dataset
uspto-grants-1995_01
Patent number
US05380850

Reaction notes

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