2-Aminopropanol → 1-[5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-3-[2-(4-methyl-oxazol-2-yl)-ethyl]-urea
Reaction equation
[CH2:1]([C:3]1[O:7][C:6]([CH2:8][CH2:9][NH:10][C:11]([NH:13][C:14]2[S:15][C:16]([C:20]3[CH:25]=[CH:24][C:23]([S:26]([CH3:29])(=[O:28])=[O:27])=[C:22]([F:30])[CH:21]=3)=[C:17]([CH3:19])[N:18]=2)=[O:12])=[N:5]C=1)[CH3:2].C(C1OC(CCN)=NC=1)C.CC1N=C(CCN)OC=1.Cl.C(C1OC(CCN)=NC=1)C.NCC(O)CC.NC(C)CO>>[F:30][C:22]1[CH:21]=[C:20]([C:16]2[S:15][C:14]([NH:13][C:11]([NH:10][CH2:9][CH2:8][C:6]3[O:7][CH:3]=[C:1]([CH3:2])[N:5]=3)=[O:12])=[N:18][C:17]=2[CH3:19])[CH:25]=[CH:24][C:23]=1[S:26]([CH3:29])(=[O:28])=[O:27]Participants
7
Reactant 6
Product 1
Procedure
The title compound is prepared by the same procedure as 1-[2-(5-ethyl-oxazol-2-yl)-ethyl]-3-[5-(3-fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-urea (Example 178) by replacing 2-(5-ethyl-oxazol-2-yl)-ethylamine hydrochloride (step 4) with the hydrochloride salt of 2-(4-methyl-oxazol-2-yl)ethylamine. This is prepared by the same procedure as 2-(5-ethyl-oxazol-2-yl)-ethylamine hydrochloride (step 4) by replacing 1-amino-2-butanol (step 1) with 2-amino-1-propanol.
Sources & evidence
- ORD record
- ord-f04f48aca45e46f2914260fe53cf66df
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129541B2
Reaction notes
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