Tetrahydrofurfurylamine → HCID 67091841, compound

HRID 1819183Notes

Reaction equation

HRID 1819183 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:28]([F:31])([F:30])[F:29])=[C:6]([CH:27]=1)[CH2:7][N:8]1[CH2:13][CH2:12][NH:11][C:10]2[N:14]=[CH:15][C:16]([C:18]3[CH:19]=[C:20]([CH:24]=[CH:25][CH:26]=3)[C:21]([OH:23])=O)=[CH:17][C:9]1=2.[NH2:32][CH2:33][CH:34]1[CH2:38][CH2:37][CH2:36][O:35]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:28]([F:29])([F:31])[F:30])=[C:6]([CH:27]=1)[CH2:7][N:8]1[CH2:13][CH2:12][NH:11][C:10]2[N:14]=[CH:15][C:16]([C:18]3[CH:19]=[C:20]([CH:24]=[CH:25][CH:26]=3)[C:21]([NH:32][CH2:33][CH:34]3[CH2:38][CH2:37][CH2:36][O:35]3)=[O:23])=[CH:17][C:9]1=2

Participants

3

Procedure

3-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with 2-(aminomethyl)tetrahydrofuran as in General Procedure 10 to give the title compound. LCMS: m/z=530.97 (M+H+); retention time=0.81 minutes.

Sources & evidence

ORD record
ord-9fc5fe6daeee49d0b84a176fd1697629
Source dataset
uspto-grants-2009_10
Patent number
US07601716B2

Reaction notes

Loading…