Methyl bromoacetate → HCID 58978333, compound

HRID 2115426Notes

Reaction equation

HRID 2115426 reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:14][C:15]2[CH:16]=[CH:17][C:18]([NH:21]C(=O)C)=[N:19][CH:20]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].Br[CH2:26][C:27]([O:29]C)=[O:28]>>[NH2:21][C:18]1[N:19]=[CH:20][C:15]([N:14]([CH2:26][C:27]([OH:29])=[O:28])[S:11]([C:8]2[CH:9]=[CH:10][C:5]([C:1]([CH3:3])([CH3:4])[CH3:2])=[CH:6][CH:7]=2)(=[O:13])=[O:12])=[CH:16][CH:17]=1

Participants

3

Reactant 2

HCID 60984Methyl bromoacetateHCID 58978317HCID 58978317, compound

Product 1

HCID 58978333HCID 58978333, compound

Procedure

prepared by reaction of N-[5-(4-tert-butyl-benzenesulfonylamino)-pyridin-2-yl]-acetamide with methyl bromoacetate

Sources & evidence

ORD record
ord-a71da2f796bd485c8e518e128e0a07d8
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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