2-(Ethylamino)ethanol → HCID 89906420, compound

HRID 525683Notes

Reaction equation

HRID 525683 reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[C:6]([CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][C:17]([F:20])([F:19])[F:18])=[CH:12][CH:11]=1)=[O:8].[CH2:23]([NH:25][CH2:26][CH2:27][OH:28])[CH3:24]>>[Br:1][C:2]1[C:3]([N:25]([CH2:23][CH3:24])[CH2:26][CH2:27][OH:28])=[N:4][CH:5]=[C:6]([CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][C:17]([F:20])([F:19])[F:18])=[CH:12][CH:11]=1)=[O:8]

Participants

3

Reactant 2

HCID 80722-(Ethylamino)ethanolHCID 867026055-bromo-6-chloro-N-(4-((trifluoromethyl)thio)phenyl)nicotinamide

Product 1

HCID 89906420HCID 89906420, compound

Procedure

The title compound was prepared in an analogous fashion to that described in Stage 22.1 using 5-bromo-6-chloro-N-(4-((trifluoromethyl)thio)phenyl)nicotinamide (Stage 25.2) and 2-ethylamino-ethanol to afford a white crystalline solid. HPLC (Condition 4) tR=6.33 min, UPLC-MS (Condition 3) tR=1.25 min, m/z=466.2 [M+H]+.

Workup

  1. customto afford a white crystalline solid

Sources & evidence

ORD record
ord-7e610ce70edf43d6a8faae571c080622
Source dataset
uspto-grants-2016_05
Patent number
US09340537B2

Reaction notes

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