Exo-2-bornanamine → HCID 18617678, compound

HRID 1264279Notes

Reaction equation

HRID 1264279 reaction equation
[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH2:3][CH:2]2[NH2:8].[C:9]([C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([CH2:20][CH2:21][NH:22][C:23](=[O:37])[C:24]3[CH:29]=[CH:28][C:27]([C:30]4[CH:35]=[CH:34][N:33]=[C:32](Cl)[N:31]=4)=[CH:26][CH:25]=3)[CH:18]=2)[NH:13][CH:12]=1)#[N:10]>>[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH2:3][CH:2]2[NH:8][C:32]1[N:31]=[C:30]([C:27]2[CH:26]=[CH:25][C:24]([C:23]([NH:22][CH2:21][CH2:20][C:17]3[CH:18]=[C:19]4[C:14](=[CH:15][CH:16]=3)[NH:13][CH:12]=[C:11]4[C:9]#[N:10])=[O:37])=[CH:29][CH:28]=2)[CH:35]=[CH:34][N:33]=1

Participants

3

Procedure

Using Bicyclo[2.2.1]hept-2-ylamine and N-[2-(3-Cyano-1H-indol-5-yl)-ethyl]-4-[2-chloro-pyrimidin-4-yl]-benzamide (reference example 1az) as substrates. MS (ion spray) m/z 477 (M+H)+.

Sources & evidence

ORD record
ord-774605873e4d4d659b4c0604133a969b
Source dataset
uspto-grants-2003_04
Patent number
US06541505B1

Reaction notes

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