3-Pentanamine → HCID 57880837, compound
Reaction equation
Cl[C:2]1[C:3]([NH2:12])=[N:4][C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[NH2:13][CH:14]([CH2:17][CH3:18])[CH2:15][CH3:16]>>[CH3:16][CH2:15][CH:14]([NH:13][C:2]1[C:3]([NH2:12])=[N:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[N:11]=1)[CH2:17][CH3:18]Participants
3
Conditions
- Temperature
- 120 °C
Procedure
A thick-walled microwave bottle equipped with a stirbar was charged with 3-chloroquinoxalin-2-amine (1.0 equiv) and 20 volume equivalents of 3-aminopentane. The bottle was fitted with a septum and cap and heated to 120° C. in a microwave for 30 min. The resulting solution was concentrated in vacuo. Flash chromatography (20%-60% EtOAc/Hexanes) provided the title compound (78%) as a yellow solid. LCMS m/z (APCI)=231.1 (M+H).
Workup
- customA thick-walled microwave bottle equipped with a stirbar
- customThe bottle was fitted with a septum
- customcap
- concentrationThe resulting solution was concentrated in vacuo
Sources & evidence
- ORD record
- ord-1e61282e350a48feaf37d6470e9eb49d
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08716291B2
Reaction notes
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