1-(2-(Benzyloxy)-3-fluorophenyl)cyclopropanamine → HCID 66689174, compound

HRID 337122Notes

Reaction equation

HRID 337122 reaction equation
[CH2:1]([O:8][C:9]1[C:14]([F:15])=[CH:13][CH:12]=[CH:11][C:10]=1[C:16]1([NH2:19])[CH2:18][CH2:17]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[C:21]1[C:22](=[O:39])[N:23]([C:28]2[CH:29]=[C:30]([CH:35]=[CH:36][C:37]=2[CH3:38])[C:31]([O:33][CH3:34])=[O:32])[CH:24]=[C:25]([Br:27])[N:26]=1>>[CH2:1]([O:8][C:9]1[C:14]([F:15])=[CH:13][CH:12]=[CH:11][C:10]=1[C:16]1([NH:19][C:21]2[C:22](=[O:39])[N:23]([C:28]3[CH:29]=[C:30]([CH:35]=[CH:36][C:37]=3[CH3:38])[C:31]([O:33][CH3:34])=[O:32])[CH:24]=[C:25]([Br:27])[N:26]=2)[CH2:18][CH2:17]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Procedure

Prepared using a similar method to Example 252h from 1-(2-(benzyloxy)-3-fluorophenyl)cyclopropanamine (Example 283b) and methyl 3-(3,5-dibromo-2-oxopyrazin-1(2H)-yl)-4-methylbenzoate (Example 252g).

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-560caa0f2c0f4ad0be5807e2ab23550a
Source dataset
uspto-grants-2014_11
Patent number
US08889692B2

Reaction notes

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