Реакция #71691

Уравнение реакции

(3S)-3-Methyl-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine

HATU

6-fluoro-4-methyl-3-pyridinecarboxylic acid

DIPEA

→

title compound

Выход 100.0%

(2S)-1-[(6-Fluoro-4-methyl-3-pyridinyl)carbonyl]-2-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine

Выход 100.0%

Растворители

DMF

Условия реакции

Обработка

1. 1
   workup.STIRRINGstirring
2. 2
   workup.WAITwas continued for 1.25 h
3. 3
   ДругоеThe reaction mixture was partitioned between DCM and saturated aqueous NaHCO3 solution (20 ml each)
4. 4
   ДругоеThe layers were separated
5. 5
   Промывкаthe aqueous was washed with further DCM (2×20 ml)
6. 6
   КонцентрированиеThe combined organic layers were concentrated
7. 7
   Другоеto leave a dark brown gum
8. 8
   ДругоеPurification by silica chromatography (Biotage SP4, 25S cartridge)
9. 9
   Промывкаeluting with 12-100% ethyl acetate in hexanes

Методика

HATU (440 mg, 1.16 mmol) was added to a solution of 6-fluoro-4-methyl-3-pyridinecarboxylic acid (supplied by Frontier Scientific) (150 mg, 0.97 mmol) in DMF (4 ml) and the mixture was treated with DIPEA (0.422 ml, 2.42 mmol). This mixture was stirred for ca. 10 min at ambient temperature. (3S)-3-Methyl-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (may be prepared as described in Description 2) (358 mg, 1.16 mmol) was added and stirring was continued for 1.25 h. The reaction mixture was partitioned between DCM and saturated aqueous NaHCO3 solution (20 ml each). The layers were separated and the aqueous was washed with further DCM (2×20 ml). The combined organic layers were concentrated to leave a dark brown gum. Purification by silica chromatography (Biotage SP4, 25S cartridge), eluting with 12-100% ethyl acetate in hexanes, gave the title compound (432 mg) as a yellow gum.

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