2-(3-Bromophenyl)ethan-1-ol → HCID 86754134, compound

HRID 1416783Notes

Reaction equation

HRID 1416783 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]([OH:29])[CH2:9][NH:10][CH:11]([CH3:28])[CH2:12][C:13]2[CH:27]=[CH:26][C:16]3[O:17][C:18]([C:23]([OH:25])=[O:24])([C:20]([OH:22])=[O:21])[O:19][C:15]=3[CH:14]=2)[CH:5]=[CH:6][CH:7]=1.[Br:30][C:31]1[CH:32]=[C:33]([CH2:37][CH2:38]O)[CH:34]=[CH:35][CH:36]=1>>[ClH:1].[Br:30][C:31]1[CH:32]=[C:33]([CH2:37][CH2:38][O:24][C:23]([C:18]2([C:20]([O:22][CH2:38][CH2:37][C:33]3[CH:34]=[CH:35][CH:36]=[C:31]([Br:30])[CH:32]=3)=[O:21])[O:17][C:16]3[CH:26]=[CH:27][C:13]([CH2:12][C@H:11]([NH:10][CH2:9][C@@H:8]([C:4]4[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=4)[OH:29])[CH3:28])=[CH:14][C:15]=3[O:19]2)=[O:25])[CH:34]=[CH:35][CH:36]=1

Participants

3

Procedure

The title compound was prepared as a brown oil from 5-{2-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-propyl}-benzo[1,3]dioxole-2,2-dicarboxylic acid and 2-(3-bromophenyl)ethanol according to the procedure of Example 1; 1H NMR (300 MHz, CDCl3): δ 1.12 (m, J=6.3 Hz, 3H), 2.79 (m, 8H), 3.5 (m 2H), 4.18 (s, 1H, OH), 5.56 (m, 1H), 6.8 (m, 3H), 7.0 (m, 4H), 7.33 (m, 4H), 7.5 (m, 4H), 8.5 (m, 1H, NH); MS (ES) m/z (relative intensity): 788 (M+ +H, 100).

Sources & evidence

ORD record
ord-516814bbfa554c2e816eb8c041811488
Source dataset
uspto-grants-1999_06
Patent number
US05914339

Reaction notes

Loading…