4-Amino-1-methylpiperidine → HCID 57385386, compound

HRID 407045Notes

Reaction equation

HRID 407045 reaction equation
[F:1][C:2]([F:34])([F:33])[CH2:3][NH:4][C:5]([NH:7][C:8]1[CH:9]=[C:10]([C:14]2[N:18]3[N:19]=[CH:20][C:21]([C:23]4[CH:24]=[N:25][N:26]([CH:28]([CH3:32])[C:29](O)=[O:30])[CH:27]=4)=[CH:22][C:17]3=[N:16][CH:15]=2)[CH:11]=[CH:12][CH:13]=1)=[O:6].[CH3:35][N:36]1[CH2:41][CH2:40][CH:39]([NH2:42])[CH2:38][CH2:37]1.C1C=NC=C(C2NC(C(F)(F)F)=CN=2)C=1>>[CH3:35][N:36]1[CH2:41][CH2:40][CH:39]([NH:42][C:29](=[O:30])[CH:28]([N:26]2[CH:27]=[C:23]([C:21]3[CH:20]=[N:19][N:18]4[C:14]([C:10]5[CH:11]=[CH:12][CH:13]=[C:8]([NH:7][C:5]([NH:4][CH2:3][C:2]([F:33])([F:34])[F:1])=[O:6])[CH:9]=5)=[CH:15][N:16]=[C:17]4[CH:22]=3)[CH:24]=[N:25]2)[CH3:32])[CH2:38][CH2:37]1

Participants

4

Reactant 3

HCID 27375314-Amino-1-methylpiperidineHCID 124055183-[5-(Trifluoromethyl)-1H-imidazol-2-yl]pyridineHCID 679802202-(4-{3-[3-({[(2,2,2-trifluoroethyl)amino]carbonyl}amino)phenyl]imidazo[1,2-b]pyridazin-7-yl}-1H-pyrazol-1-yl)propanoic acid

Product 1

HCID 57385386HCID 57385386, compound

Procedure

This compound was prepared by using procedures analogous to those described for the synthesis of Example 54, Step 3 starting from 2-(4-{3-[3-({[(2,2,2-trifluoroethyl)amino]carbonyl}amino)phenyl]imidazo[1,2-b]pyridazin-7-yl}-1H-pyrazol-1-yl)propanoic acid and 1-methylpiperidin-4-amine (ABCR and Cat. No. MK534). LCMS (M+H)+: m/z=570.2.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-3fb011bb22ef44fda6a0dc70e6232de7
Source dataset
uspto-grants-2014_06
Patent number
US08754114B2

Reaction notes

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