Methyl iodide → HCID 20437873, compound

HRID 1980052Notes

Reaction equation

HRID 1980052 reaction equation
CI.[CH2:3]([O:10]C1C=CC(CCl)=CC=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:19]([CH:27]1[C:32](=[O:33])[NH:31][CH2:30][CH2:29][N:28]1[C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])(=O)C1C=CC=CC=1>>[C:3]([C:27]1([CH3:19])[C:32](=[O:33])[NH:31][CH2:30][CH2:29][N:28]1[C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])(=[O:10])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1

Participants

4

Reactant 3

HCID 6328Methyl iodideHCID 700424-Benzyloxybenzyl chlorideHCID 20437866HCID 20437866, compound

Product 1

HCID 20437873HCID 20437873, compound

Procedure

When in the procedure of Example 3a, methyl iodide is substituted for p-benzyloxybenzyl chloride and 27d is substituted for 2, the title compound is obtained.

Sources & evidence

ORD record
ord-dc14d81d61b1409d80d2e7b217af1cdd
Source dataset
uspto-grants-1984_11
Patent number
US04483988

Reaction notes

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