Methyl bromoacetate → HCID 10071071, compound

HRID 257636Notes

Reaction equation

[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([CH2:16][CH2:17][C:18]2[CH:19]=[C:20]([OH:24])[CH:21]=[CH:22][CH:23]=2)[O:9][C:10]=1[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1.Br[CH2:26][C:27]([O:29][CH3:30])=[O:28]>>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([CH2:16][CH2:17][C:18]2[CH:19]=[C:20]([CH:21]=[CH:22][CH:23]=2)[O:24][CH2:26][C:27]([O:29][CH3:30])=[O:28])[O:9][C:10]=1[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1

Participants

Reactant 2

HCID 60984Methyl bromoacetate

HCID 19783606HCID 19783606, compound

Product 1

HCID 10071071HCID 10071071, compound

Procedure

Reaction of 3-[2-[4,5-di(2-thienyl)-2-oxazolyl]-ethyl]phenol with methyl bromoacetate according to the procedure of Example 29 provided the title compound.

Sources & evidence

ORD record: ord-e654e6c88d71489fac41b7fead909209
Source dataset: uspto-grants-1993_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05262540

Reaction notes

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