2-Chloro-5-phenyloxazole → HCID 59643116, compound

HRID 2251559Notes

Reaction equation

HRID 2251559 reaction equation
[CH:1]1([C:4]2[O:8][N:7]=[C:6]([C:9]3[CH:36]=[CH:35][C:12]([CH2:13][NH:14][CH2:15][CH2:16][CH2:17][C:18]4[CH:19]=[C:20]([CH:32]=[CH:33][CH:34]=4)[O:21][C:22]([CH3:31])([CH3:30])[C:23]([O:25]C(C)(C)C)=[O:24])=[CH:11][CH:10]=3)[N:5]=2)[CH2:3][CH2:2]1.Cl[C:38]1[O:39][C:40]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)=[CH:41][N:42]=1>>[CH:1]1([C:4]2[O:8][N:7]=[C:6]([C:9]3[CH:10]=[CH:11][C:12]([CH2:13][N:14]([C:38]4[O:39][C:40]([C:43]5[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=5)=[CH:41][N:42]=4)[CH2:15][CH2:16][CH2:17][C:18]4[CH:19]=[C:20]([CH:32]=[CH:33][CH:34]=4)[O:21][C:22]([CH3:30])([CH3:31])[C:23]([OH:25])=[O:24])=[CH:35][CH:36]=3)[N:5]=2)[CH2:2][CH2:3]1

Participants

3

Reactant 2

HCID 109976262-Chloro-5-phenyloxazoleHCID 59643328HCID 59643328, compound

Product 1

HCID 59643116HCID 59643116, compound

Procedure

Similarly prepared from tert-butyl 2-[3-(3-{[4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)benzyl]amino}propyl)phenoxy]-2-methylpropanoate and 2-chloro-5-phenyl-oxazole (ref. GB1552125).

Sources & evidence

ORD record
ord-250f9ca4d98d4c77bbcc3d3568c437d6
Source dataset
uspto-grants-2008_01
Patent number
US07319104B2

Reaction notes

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