反応 #162509

反応方程式

(S)-1-(1-Methyl-6-(pyridin-2-yl)-1H-pyrrolo[3,2-b]pyridin-5-yl)ethanamine hydrochloride

2-amino-4-chloro-6-methylpyrimidine-5-carbonitrile

N-ethyl-N-isopropylpropan-2-amine

→

title compound

収率 29.0%

(S)-2-Amino-4-methyl-6-((1-(1-methyl-6-(pyridin-2-yl)-1H-pyrrolo[3,2-b]pyridin-5-yl)ethyl)amino)pyrimidine-5-carbonitrile

収率 29.0%

溶媒

acetonitrile

反応条件

後処理

1. 1
   濃縮concentrated
2. 2
   その他purified by preparative HPLC (basic mode)
3. 3
   洗浄eluting with 20-35% ACN in water
4. 4
   workup.ADDITIONThe fractions containing the desired compound
5. 5
   濃縮concentrated in vacuo
6. 6
   その他further purified by preparative HPLC (acid mode)
7. 7
   洗浄eluting with 1-25% ACN in water
8. 8
   workup.ADDITIONThe fractions containing the desired compound
9. 9
   抽出extracted with EtOAc (200 mL)
10. 10
    乾燥dried over Na2SO4
11. 11
    濃縮concentrated in vacuo

実験手順

(S)-1-(1-Methyl-6-(pyridin-2-yl)-1H-pyrrolo[3,2-b]pyridin-5-yl)ethanamine hydrochloride (151 mg, 0.522 mmol), 2-amino-4-chloro-6-methylpyrimidine-5-carbonitrile (80 mg, 0.475 mmol), and N-ethyl-N-isopropylpropan-2-amine (0.248 mL, 1.42 mmol) were combined in acetonitrile (6 mL). The reaction mixture was heated in a microwave reactor at 120° C. for 2 hours and then concentrated. The residue was taken up in DMF and purified by preparative HPLC (basic mode) eluting with 20-35% ACN in water. The fractions containing the desired compound were combined and concentrated in vacuo. The residue was taken up in DMF and further purified by preparative HPLC (acid mode) eluting with 1-25% ACN in water. The fractions containing the desired compound were combined, neutralized with NaHCO3, and extracted with EtOAc (200 mL). The organic layers were combined, dried over Na2SO4, and concentrated in vacuo to give the title compound (53 mg, 29%). 1H NMR (500 MHz, CD3OD) δ ppm 1.34-1.41 (m, 3 H), 2.31 (d, J=1.46 Hz, 3 H), 3.88 (d, J=1.46 Hz, 3H), 5.68-5.79 (m, 1 H), 6.67 (d, J=2.44 Hz, 1 H), 7.47 (dd, J=7.32, 4.88 Hz, 1 H), 7.58-7.61 (m, 1 H), 7.67 (d, J=7.81 Hz, 1 H), 7.86 (s, 1 H), 7.99 (t, J=7.81 Hz, 1 H), 8.68-8.73 (m, 1 H); ESI-MS m/z [M+H]+ calc'd for C21H20N8, 385; found 385.

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