HCID 12622379, compound → HCID 68579332, compound

HRID 1949069Notes

Reaction equation

HRID 1949069 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[O:20][CH3:21])[CH:6]=[CH:5]2.[N:22]1([C:28]2[N:32]=[C:31]([NH2:33])[O:30][N:29]=2)[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1>>[CH3:21][O:20][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[CH2:13][NH:12][C:7]1[CH:6]=[CH:5][C:4]2[C:9](=[CH:10][CH:11]=[C:2]([NH:33][C:31]3[O:30][N:29]=[C:28]([N:22]4[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]4)[N:32]=3)[CH:3]=2)[N:8]=1

Participants

3

Reactant 2

HCID 12622379HCID 12622379, compoundHCID 68574436HCID 68574436, compound

Product 1

HCID 68579332HCID 68579332, compound

Procedure

The title compound, light brown foam, MS: m/e=431.3 (M+H+), was prepared in accordance with the general method of example 84 from (6-bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amine (see example 2, step A) and 3-(piperidin-1-yl)-[1,2,4]oxadiazol-5-yl-amine [CAS-No. 75565-19-4].

Sources & evidence

ORD record
ord-a6b7eec2d2904788a8a6212aba9a1205
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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