Réaction #40277

Équation de réaction

butanone

3-[5-(2,2-dimethylpropionylamino)-pyrazin-2-yl]-3-oxo-propionic acid-tert-butyl ester

3-[5-(2,2-dimethyl-propionylamino)-pyrazin-2-yl]-3-oxo-propionic acid-tert-butyl ester

N-bromosuccinimide

→

title compound

2-bromo-3-[5-(2,2-dimethyl-propionylamino)-pyrazin-2-yl]-3-oxo-propionic acid tert-butyl ester

Solvants

butanone

Conditions de réaction

Traitement

1. 1
   AutreA 1-L round bottomed flask equipped with a magnetic stirrer
2. 2
   Autrereaction
3. 3
   ConcentrationThe reaction mixture was concentrated at 25° C./25 mmHg to a volume of ca. 70 mL
4. 4
   workup.ADDITIONdiluted with 130 mL of ethyl acetate
5. 5
   Lavagewashed with 3×100 mL L of water
6. 6
   ConcentrationAfter concentration at 35° C./60 mmHg to a volume of ca. 90 mL
7. 7
   workup.ADDITIONthe resulting suspension was diluted with 200 mL of heptane
8. 8
   Concentrationre-concentrated to a volume of ca. 90 mL
9. 9
   workup.ADDITIONThen, 200 mL of heptane was added
10. 10
    Concentrationthe suspension was again concentrated to a volume of ca, 150 mL
11. 11
    FiltrationThe solid was then collected by filtration
12. 12
    Lavagewashed with 2×50 mL of heptane
13. 13
    Autredried by suction

Mode opératoire

A 1-L round bottomed flask equipped with a magnetic stirrer was charged with 73.00 mg (0.841 mmol) of lithium bromide and the butanone solution obtained in step 3 (ca. 100 mL), which theoretically contained 27.09 g (84.30 mmol) of 3-[5-(2,2-dimethyl-propionylamino)-pyrazin-2-yl]-3-oxo-propionic acid-tert-butyl ester and ca. 73 mL of butanone. To the resulting mixture was added a total of 15.16 g (85.17 mmol) of N-bromosuccinimide portionwise with careful reaction monitoring by HPLC. After stirring at room temperature for 1 h, HPLC analysis indicated complete reaction. The reaction mixture was concentrated at 25° C./25 mmHg to a volume of ca. 70 mL, then diluted with 130 mL of ethyl acetate and washed with 3×100 mL L of water. After concentration at 35° C./60 mmHg to a volume of ca. 90 mL, the resulting suspension was diluted with 200 mL of heptane, and re-concentrated to a volume of ca. 90 mL. Then, 200 mL of heptane was added, and the suspension was again concentrated to a volume of ca, 150 mL. The solid was then collected by filtration, washed with 2×50 mL of heptane and dried by suction to give 32.16 g of the title compound as a light yellow solid; 98.7% pure as determined by HPLC analysis (HPLC column Zorbax XDB-C8, 3×100 mm, 3.5 μm, eluent 20-100% acetonitrile/water+01. % TFA over 10 min at 0.5 mL/min, detection at UV 254 nm, retention time 9.52 min).

Source