HCID 13154139, compound → HCID 22403075, compound

HRID 259757Notes

Reaction equation

HRID 259757 reaction equation
[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][C:4]=1[C:11]1[NH:12][CH:13]=[CH:14][CH:15]=1.C(S(C1[CH:22]=[CH:23][C:24](OC)=[C:25]([C:27]2[NH:28][CH:29]=CC=2)C=1)(=O)=O)C>>[CH3:1][O:2][C:3]1[C:8]([O:9][CH3:10])=[CH:7][CH:6]=[CH:5][C:4]=1[C:11]1[NH:12][C:13]([CH2:29][N:28]2[CH2:27][CH2:25][CH2:24][CH2:23][CH2:22]2)=[CH:14][CH:15]=1

Participants

3

Reactant 2

HCID 13154139HCID 13154139, compoundHCID 139003532-[5-(Ethanesulfonyl)-2-methoxyphenyl]-1H-pyrrole

Product 1

HCID 22403075HCID 22403075, compound

Procedure

This compound was prepared by a method analogous to that used to prepare example 2, but using 2-(2,3-dimethoxyphenyl)-1H-pyrrole (prepared according to the method of Kruse et al., [Heterocycles, 26, 3141, 1987] from the corresponding acid chloride) in place of 2-(5-ethylsulphonyl-2-methoxyphenyl)-1H-pyrrole.

Workup

  1. customThis compound was prepared by a method analogous to
  2. customto prepare example 2
  3. customprepared

Sources & evidence

ORD record
ord-c03593551de041498efb7c4f2a697ece
Source dataset
uspto-grants-1996_06
Patent number
US05523299

Reaction notes

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