4-Amino-1-butanol → HCID 24997655, compound

HRID 659007

Reaction equation

HRID 659007 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][C:19]3[CH:24]=[CH:23][N:22]=[C:21](S(C)(=O)=O)[N:20]=3)=[CH:14][CH:13]=2)=[O:10])=[CH:4][C:3]=1[C:29]([F:32])([F:31])[F:30].[NH2:33][CH2:34][CH2:35][CH:36]([OH:38])[CH3:37].NCCCCO>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][C:19]3[CH:24]=[CH:23][N:22]=[C:21]([NH:33][CH2:34][CH2:35][CH:36]([OH:38])[CH3:37])[N:20]=3)=[CH:14][CH:13]=2)=[O:10])=[CH:4][C:3]=1[C:29]([F:32])([F:31])[F:30]

Participants

4

Reactant 3

HCID 258684-Amino-1-butanolHCID 1702542-Butanol, 4-amino-HCID 67523920HCID 67523920, compound

Product 1

HCID 24997655HCID 24997655, compound

Procedure

The compound was prepared from 1-(4-Chloro-3-trifluoromethyl-phenyl)-3-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-phenyl]-urea and 4-amino-butan-2-ol as described in example 10 for 4-amino-butan-1-ol instead.

Sources & evidence

ORD record
ord-06a37e85bbef4f9e8561b9c2e1c85ca2
Source dataset
uspto-grants-2011_12
Patent number
US08080552B2

Linked notes

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