1-(Methoxymethyl)cyclopropanemethanamine → HCID 178494605, compound

HRID 578997Notes

Reaction equation

HRID 578997 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19](O)=[O:20])=[CH:17][N:16]=3)[C:13]=2[OH:14])=[C:5]([CH3:24])[CH:4]=1)#[N:2].[CH3:25][O:26][CH2:27][C:28]1([CH2:31][NH2:32])[CH2:30][CH2:29]1>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][N:12]([C:15]3[CH:23]=[CH:22][C:18]([C:19]([NH:32][CH2:31][C:28]4([CH2:27][O:26][CH3:25])[CH2:30][CH2:29]4)=[O:20])=[CH:17][N:16]=3)[C:13]=2[OH:14])=[C:5]([CH3:24])[CH:4]=1)#[N:2]

Participants

3

Reactant 2

HCID 280645641-(Methoxymethyl)cyclopropanemethanamineHCID 178426451HCID 178426451, compound

Product 1

HCID 178494605HCID 178494605, compound

Procedure

The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-(methoxymethyl)cyclopropyl)methanamine 1H NMR (400 MHz, DMSO-d6) δ ppm 0.36-0.44 (m, 2 H) 0.52-0.60 (m, 2 H) 2.43 (s, 3 H) 3.22-3.28 (m, 5 H) 3.35 (s, 2 H) 7.66 (d, J=7.83 Hz, 1 H) 7.73 (s, 1 H) 7.77 (br. s., 1 H) 8.08-8.26 (m, 1 H) 8.42 (d, J=6.57 Hz, 2 H) 8.64 (t, J=5.56 Hz, 1 H) 8.88-8.94 (m, 1 H) 12.96-13.46 (m, 1 H). MS m/z [M+H]+ 418.2

Sources & evidence

ORD record
ord-4db9ba770ac54f54a7b74bb17c08e12d
Source dataset
uspto-grants-2015_05
Patent number
US09040522B2

Reaction notes

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