HCID 23436472, compound → HCID 10805572, compound

HRID 2121208Notes

Reaction equation

HRID 2121208 reaction equation
[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[CH:6][C:5]=1OS(C(F)(F)F)(=O)=O.I[C:28]1[CH:36]=[C:35](C([O-])=O)[CH:34]=[CH:33][C:29]=1C([O-])=O>>[CH3:1][O:2][C:3](=[O:26])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[CH:6][C:5]=1[C:28]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:29]=1

Participants

3

Reactant 2

HCID 23436472HCID 23436472, compoundHCID 54262279HCID 54262279, compound

Product 1

HCID 10805572HCID 10805572, compound

Procedure

The desired compound was prepared according to the method of Example 158A, except substituting 4-(3-pyridylmethyloxy)-2-trifluoromethanesulfonyloxybenzoic acid methyl ester, prepared as in Example 240C for 2-iodoterephthalate.

Sources & evidence

ORD record
ord-2182b18791a443f584e243031186c41c
Source dataset
uspto-grants-2004_02
Patent number
US06693123B2

Reaction notes

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