3-amino-N-propylbenzamide → HCID 86600722, compound

HRID 734081Notes

Reaction equation

HRID 734081 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8]C2C=CC=C(O)C=2)[C:5](F)=[CH:4][N:3]=1.[CH2:17]([NH:20][C:21]([C:23]1[CH:24]=[C:25]([CH:27]=[CH:28][CH:29]=1)[NH2:26])=[O:22])[CH2:18][CH3:19]>>[CH2:17]([NH:20][C:21]([C:23]1[CH:24]=[C:25]([NH:26][C:2]2[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][N:3]=2)[CH:27]=[CH:28][CH:29]=1)=[O:22])[CH2:18][CH3:19]

Participants

3

Reactant 2

HCID 129616703-amino-N-propylbenzamideHCID 220604512-chloro-5-fluoro-N-(3-hydroxyphenyl)-4-pyrimidineamine

Product 1

HCID 86600722HCID 86600722, compound

Procedure

In like manner to the preparation of 5-fluoro-N4-(3-hydroxyphenyl)-N2-[4-(3-phenyl-1,2,4-oxadiazol-5-yl)methyleneoxyphenyl]-2,4-pyrimidinediamine, 2-chloro-5-fluoro-N4-(3-hydroxyphenyl)-4-pyrimidineamine and 3-[(N-propylamino)carbonyl]aniline were reacted to provide 5-fluoro-N4-3-hydroxyphenyl)-N2-[3-[(N-propylamino)carbonyl]phenyl]-2,4-pyrimidinediamine. 1H NMR (CD3OD): δ 8.00 (d, 1H, J=5.4 Hz), 7.84 (t, 1H, J=1.8 Hz), 7.69–7.59 (m, 2H), 7.44 (t, 1H, J=7.5 Hz), 7.16–7.05 (m, 3H), 6.67 (td, 1H, J=2.4 and 7.2 Hz), 3.34–3.29 (m, 2H), 1.65–1.56 (m, 2H), 0.96 (t, 3H, J=7.5 Hz); 19F NMR (282 MHz, CD3OD): −46049; LCMS: purity: 94%; MS (m/e): 382(MH+).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-79fd8176203e440e9be655a3549215d5
Source dataset
uspto-grants-2009_09
Patent number
US07589200B2

Reaction notes

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