Pyrrolidine → HCID 58894267, compound

HRID 2263940Notes

Reaction equation

HRID 2263940 reaction equation
[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([S:10](Cl)(=[O:12])=[O:11])[C:7]([O:14][CH3:15])=[CH:6][C:5]=1[O:16][CH2:17][CH3:18].[NH:20]1[CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([S:10]([N:20]2[CH2:24][CH2:23][CH2:22][CH2:21]2)(=[O:12])=[O:11])[C:7]([O:14][CH3:15])=[CH:6][C:5]=1[O:16][CH2:17][CH3:18]

Participants

3

Reactant 2

HCID 31268PyrrolidineHCID 866128795-Chlorosulfonyl-2-ethoxy-4-methoxy-benzoic acid methyl ester

Product 1

HCID 58894267HCID 58894267, compound

Procedure

In a manner analogous to the method described in example 33, 5-chlorosulfonyl-2-ethoxy-4-methoxy-benzoic acid methyl ester was reacted with pyrrolidine to give the title compound.

Sources & evidence

ORD record
ord-58b11b39e9734c1193163110edb03f7a
Source dataset
uspto-grants-2010_12
Patent number
US07851626B2

Reaction notes

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