Sesamol → ethyl [4-bromo-3-hydroxy-3-(6-hydroxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-2-oxo-2,3-dihydro-1H-indol-1-yl]acetate

HRID 645052Notes

Reaction equation

HRID 645052 reaction equation
C1(CCN2C3C(=CC=CC=3)C(=O)C2=O)CC1.[CH2:17]([O:19][C:20](=[O:34])[CH2:21][N:22]1[C:30]2[C:25](=[C:26]([Br:31])[CH:27]=[CH:28][CH:29]=2)[C:24](=[O:32])[C:23]1=[O:33])[CH3:18].O1C2C=CC(O)=CC=2OC1.[CH3:45][C:46]1([CH3:56])[CH2:50][C:49]2[CH:51]=[CH:52][C:53]([OH:55])=[CH:54][C:48]=2[O:47]1>>[CH2:17]([O:19][C:20](=[O:34])[CH2:21][N:22]1[C:30]2[C:25](=[C:26]([Br:31])[CH:27]=[CH:28][CH:29]=2)[C:24]([OH:32])([C:52]2[C:53]([OH:55])=[CH:54][C:48]3[O:47][C:46]([CH3:56])([CH3:45])[CH2:50][C:49]=3[CH:51]=2)[C:23]1=[O:33])[CH3:18]

Participants

5

Procedure

Following the procedure as described in PREPARATION 2B, and making non-critical variations to replace 1-(2-cyclopropylethyl)-1H-indole-2,3-dione with ethyl(4-bromo-2,3-dioxo-2,3-dihydro-1H-indol-1-yl)acetate and 1,3-benzodioxol-5-ol with 2,2-dimethyl-2,3-dihydrobenzofuran-6-ol, the title compound was obtained: MS (ES+) m/z 498.5 (M+23), 500.5 (M+23).

Sources & evidence

ORD record
ord-69e232dc30d54aeb94ab12d880c6e519
Source dataset
uspto-grants-2010_04
Patent number
US07700641B2

Reaction notes

Loading…