Chloroacetyl chloride → tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

To a suspension of tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (1.0 g, 2.21 mmol) in EtOAc:THF:sat'd NaHCO3 (110 mL: 30 mL: 50 mL) was added 2-chloroacetyl chloride (1 mL, 12.6 mmol) and stirred at RT for 2.5 hr. The reaction mixture was stirred at RT for 1.5 h. Another addition of 2-chloroacetyl chloride (0.5 mL) was added and continued to stir for 2 h. Concentrated in vacuo to remove volatiles and residue was washed with 5% citric acid (2×50 mL), water (2×100 mL), and sat′d NaCl (1×50 mL). The organic layer was dried under Na2SO4 and concentrated in vacuo to give the desired product tert-butyl 5-(2-(3-(2-chloroacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate. (1.02 g, 87%)

1. stirringThe reaction mixture was stirred at RT for 1.5 h
2. additionwas added
3. stirringto stir for 2 h
4. concentrationConcentrated in vacuo
5. customto remove volatiles and residue
6. washwas washed with 5% citric acid (2×50 mL), water (2×100 mL), and sat′d NaCl (1×50 mL)
7. customThe organic layer was dried under Na2SO4
8. concentrationconcentrated in vacuo

ORD-Eintrag

ord-3099372715d843929b4b51d83897dcb4

Quelldatensatz

uspto-grants-2016_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09440961B2