Basic information Safety Supplier Related

TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE

Basic information Safety Supplier Related

TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE Basic information

Product Name:
TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
Synonyms:
  • TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
  • 2-BOC-8-BROMO-1,2,3,4-TETRAHYDRO-ISOQUINOLINE
  • N-BOC-1,2,3,4-tetrahydro-8-broMo-isoquinoline
  • 2(1H)-Isoquinolinecarboxylic acid, 8-bromo-3,4-dihydro-, 1,1-dimethylethyl ester
  • N-Boc-8-Bromo-1,2,3,4-tetrahydroisoquinoline
CAS:
893566-75-1
MF:
C14H18BrNO2
MW:
312.2
Mol File:
893566-75-1.mol
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TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE Chemical Properties

Boiling point:
382.4±42.0 °C(Predicted)
Density 
1.353±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-1.60±0.20(Predicted)
Appearance
White to off-white Solid
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TERT-BUTYL 8-BROMO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE Usage And Synthesis

Uses

tert-Butyl 8-Bromo-3,4-dihydroisoquinoline-2(1H)-carboxylate is an Amide compound; having BET proteolysis-inducing action, and medicinal application thereof.

Synthesis

24424-99-5

75416-51-2

893566-75-1

Di-tert-butyl dicarbonate (Boc2O, 25.73 g, 117.88 mmol) was added slowly and dropwise at 0 °C to dichloromethane (DCM, containing 8-bromo-1,2,3,4-tetrahydroisoquinoline (Intermediate 21, 25.00 g, 117.88 mmol) and triethylamine (TEA, 32.83 mL, 236.00 mmol) in a 300 mL) solution. The reaction mixture was stirred continuously for 30 minutes at room temperature. Upon completion of the reaction, citric acid solution was added to quench the reaction, followed by a layering operation. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 3/1, v/v) to afford N-boc-8-bromo-1,2,3,4-tetrahydroisoquinoline (Intermediate 22, 35 g, 95% yield).

References

[1] Patent: WO2017/216293, 2017, A1. Location in patent: Page/Page column 74; 75

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