Propanolamine ethyl ether → HCID 77750243, compound

HRID 840715Notes

Reaction equation

HRID 840715 reaction equation
[OH:1][CH:2]1[CH:6]([OH:7])[CH:5]([N:8]2[C:12]3[N:13]=[C:14]([S:27][CH3:28])[N:15]=[C:16]([NH:17][CH:18]4[CH2:20][CH:19]4[C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)[C:11]=3[N:10]=[N:9]2)[CH2:4][CH:3]1[C:29]([NH:31][C:32]1[CH:37]=[CH:36]C=CC=1)=[O:30].[CH2:38]([O:40]CCCN)[CH3:39]>>[CH2:38]([O:40][CH2:36][CH2:37][CH2:32][NH:31][C:29]([CH:3]1[CH2:4][CH:5]([N:8]2[C:12]3[N:13]=[C:14]([S:27][CH3:28])[N:15]=[C:16]([NH:17][CH:18]4[CH2:20][CH:19]4[C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=4)[C:11]=3[N:10]=[N:9]2)[CH:6]([OH:7])[CH:2]1[OH:1])=[O:30])[CH3:39]

Participants

3

Procedure

The subtitle compound was prepared according to the method of example 39, step a) using the product of example 20, step b) and 3-ethyoxypropylamine.

Sources & evidence

ORD record
ord-15ec089c771f4270bc24751e468ce698
Source dataset
uspto-grants-2002_04
Patent number
US06369064B1

Reaction notes

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