HCID 18448357, compound → HCID 58622864, compound

Reaction equation

[Br:1][C:2]1[C:3]([CH3:13])=[C:4]([CH:10]=[CH:11][CH:12]=1)[NH:5][CH2:6][CH2:7][O:8][CH3:9].BrC1C(C)=C(N([CH2:26][C:27]2[CH:39]=[CH:38][C:30]([O:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[C:29]([CH3:40])[CH:28]=2)CCCC)C=CC=1>>[Br:1][C:2]1[C:3]([CH3:13])=[C:4]([N:5]([CH2:26][C:27]2[CH:39]=[CH:38][C:30]([O:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[C:29]([CH3:40])[CH:28]=2)[CH2:6][CH2:7][O:8][CH3:9])[CH:10]=[CH:11][CH:12]=1

Participants

Reactant 2

HCID 18448357HCID 18448357, compound

HCID 58622888HCID 58622888, compound

Product 1

HCID 58622864HCID 58622864, compound

Procedure

Prepared from 3-bromo-N-(2-methoxyethyl)-2-methylaniline using the procedure described for Intermediate 59.

Sources & evidence

ORD record: ord-6190ca839d564739871c3643152e7580
Source dataset: uspto-grants-2007_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07199239B2

Reaction notes

Loading…