2-Chlorobenzoxazole → HCID 59643395, compound

HRID 2251553Notes

Reaction equation

HRID 2251553 reaction equation
[CH:1]1([C:4]2[O:8][N:7]=[C:6]([C:9]3[CH:33]=[CH:32][C:12]([CH2:13][NH:14][CH2:15][CH2:16][C:17]4[CH:31]=[CH:30][C:20]([O:21][C:22]([CH3:29])([CH3:28])[C:23]([O:25]CC)=[O:24])=[CH:19][CH:18]=4)=[CH:11][CH:10]=3)[N:5]=2)[CH2:3][CH2:2]1.Cl[C:35]1[O:36][C:37]2[CH:43]=[CH:42][CH:41]=[CH:40][C:38]=2[N:39]=1>>[O:36]1[C:37]2[CH:43]=[CH:42][CH:41]=[CH:40][C:38]=2[N:39]=[C:35]1[N:14]([CH2:13][C:12]1[CH:11]=[CH:10][C:9]([C:6]2[N:5]=[C:4]([CH:1]3[CH2:2][CH2:3]3)[O:8][N:7]=2)=[CH:33][CH:32]=1)[CH2:15][CH2:16][C:17]1[CH:18]=[CH:19][C:20]([O:21][C:22]([CH3:29])([CH3:28])[C:23]([OH:25])=[O:24])=[CH:30][CH:31]=1

Participants

3

Reactant 2

HCID 119862-ChlorobenzoxazoleHCID 59643390HCID 59643390, compound

Product 1

HCID 59643395HCID 59643395, compound

Procedure

Similarly prepared from ethyl 2-[4-(2-{[4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)benzyl]amino}ethyl)phenoxy]-2-methylpropanoate and 2-chlorobenzoxazole.

Sources & evidence

ORD record
ord-e9cf084987804b33bb05f14d6c52ed43
Source dataset
uspto-grants-2008_01
Patent number
US07319104B2

Reaction notes

Loading…