2-(Ethylamino)ethanol → HCID 10203302, compound

HRID 347056Notes

Reaction equation

HRID 347056 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:12]3[CH:13]=[CH:14][C:15]([O:17][CH2:18][CH2:19][CH2:20]Br)=[CH:16][C:11]=3[S:10][N:9]=2)=[CH:4][CH:3]=1.[CH2:22]([NH:24][CH2:25][CH2:26][OH:27])[CH3:23]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:12]3[CH:13]=[CH:14][C:15]([O:17][CH2:18][CH2:19][CH2:20][N:24]([CH2:22][CH3:23])[CH2:25][CH2:26][OH:27])=[CH:16][C:11]=3[S:10][N:9]=2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 80722-(Ethylamino)ethanolHCID 223140693-(4-Bromo-phenyl)-6-(3-bromo-propoxy)-benzo[d]isothiazole

Product 1

HCID 10203302HCID 10203302, compound

Procedure

According to the method in example 4, 3-(4-Bromo-phenyl)-6-(3-bromo-propoxy)-benzo[d]isothiazole and 2-(ethylamino)ethanol were converted to yield 2-[[3-[3-(4-Bromo-phenyl)-benzo[d]isothiazol-6-yloxy]-propyl]-ethyl-amino]-ethanol, MS: 436 (MH+, 1Br).

Sources & evidence

ORD record
ord-5c8bed82484d4065ad7b8a9f789c4656
Source dataset
uspto-grants-2007_02
Patent number
US07173043B2

Reaction notes

Loading…