2-bromo-3-methoxy-N-(4-methylpent-2-yn-4-yl)propionamide → HCID 21078403, compound

HRID 916542Notes

Reaction equation

HRID 916542 reaction equation
[Br:1][CH:2]([CH2:12][O:13][CH3:14])[C:3]([NH:5][C:6]([CH3:11])([CH3:10])[C:7]#[C:8][CH3:9])=[O:4].Cl.NC(C)(C)C#C[CH2:20][O:21]C>>[Br:1][CH:2]([CH2:12][O:13][CH3:14])[C:3]([NH:5][C:6]([CH3:10])([CH3:11])[C:7]#[C:8][CH2:9][O:21][CH3:20])=[O:4]

Participants

3

Reactant 2

HCID 210784052-bromo-3-methoxy-N-(4-methylpent-2-yn-4-yl)propionamideHCID 219231274-Amino-1-methoxy-4-methylpent-2-yne hydrochloride

Product 1

HCID 21078403HCID 21078403, compound

Procedure

2-Bromo-N-(1-methoxy-4-methylpent-2-yn-4-yl)-3-methoxypropionamide was prepared from 2-bromo-1-methoxypropionic acid in a similar manner to 2-bromo-N-(4-methylpent-2-yn-4-yl)-3-methoxypropionamide described in Example 3, Stage 1, Step 2 using 4-amino-1-methoxy-4-methylpent-2-yne hydrochloride in place of 4-amino-4-methylpent-2-yne hydrochloride.

Sources & evidence

ORD record
ord-9e34b9dab7214d579b4c9bfaf0eb448b
Source dataset
uspto-grants-2007_09
Patent number
US07271130B2

Reaction notes

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