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1356953-69-9

1-(1-methyl-3-pyrrolidinyl)-1H-pyrazol-4-amine synthesis

4synthesis methods
1H-Pyrazole, 1-(1-methyl-3-pyrrolidinyl)-4-nitro-

1383706-07-7
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1-(1-methyl-3-pyrrolidinyl)-1H-pyrazol-4-amine

1356953-69-9
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Yield:1356953-69-9 100%

Reaction Conditions:

with palladium 10% on activated carbon;hydrogen in ethanol; for 16 h;

Steps:

21.c (C) 1-(1-Methylpyrrolidin-3-yI)- 1H-pyrazol-4-amine (A24)

(C) 1-(1-Methylpyrrolidin-3-yI)- 1H-pyrazol-4-amine (A24)A solution of 1-(1-methylpyrrolidin-3-yl)-4-nitro-1 H-pyrazole A23 (0.575 g, 2.93 mmol) and 10% Pd/C (0.061 g) in EtOH (15 mL) was stirred under a hydrogen atmosphere for 16 hours. The reaction mixture was filtered through Celite and the solvent wasremoved in vacuo to give the title compound A24 as a red oil (0.555 g, quantitative).1H NMR (300 MHz, MeOD) O 2.27-2.42 (m, 1H), 2.72- 2.76 (m, 2H), 3.02- 3.10 (m,1H), 3.46-3.55 (m, 1H), 3.70-3.85 (m, 4H), 5.14-5.26 (m, 1H), 7.33 (5, 1H), 7.46(m, 1H).

References:

WO2014/26243,2014,A1 Location in patent:Page/Page column 125