반응 #2045070

ord-c05b54ed4a4f40db8c4914b505b4a8a7

반응 방정식

CN(C)C=O
DMF
Cc1ccc2c(N=[N+]=[N-])ccc(O)c2n1
13
Cc1ccc2c(N=[N+]=[N-])ccc(O)c2n1
5-Azido-8-hydroxy-2-methylquinoline
c1c[nH]cn1
imidazole
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butyldiphenylsilyl chloride
Cc1ccc2c(N=[N+]=[N-])ccc(O[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)c2n1
protected product
Cc1ccc2c(N=[N+]=[N-])ccc(O[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)c2n1
5-Azido-8-tert-butyldiphenylsilyloxy-2-methylquinoline

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with aqueous HCl (0.1 M, 50 mL), brine (100 mL), water (100 mL)
  2. 2
    건조dried over Na2SO4
  3. 3
    기타evaporated under reduced pressure

실험 절차

A 100-mL flask was successively loaded with dry DMF (10 mL), 13 (200 mg, 1 mmol), imidazole (68.08 mg, 1 mmol), and tert-butyldiphenylsilyl chloride (302 mg, 1.1 mmol). The solution was stirred at room temperature for 10 h, diluted with ethyl acetate (500 mL), washed with aqueous HCl (0.1 M, 50 mL), brine (100 mL), water (100 mL), dried over Na2SO4 and evaporated under reduced pressure to afford 8.41 g (96%) of protected product as a colorless oil (428 mg, 98%). 1H NMR (500 MHz, CDCl3) δ ppm: 1.19 (s, 9H), 2.33 (s, 3H), 6.98 (d, J=8.5 Hz, 1H), 7.06 (d, J=8.5 Hz, 1H), 7.10 (d, J=8.5 Hz, 1H), 7.38-7.26 (m, 6H), 7.81-7.79 (m, 4H), 8.11 (d, J=8.5 Hz, 1H). 13C NMR (125 MHz, CDCl3) δ ppm: 20.1, 24.3, 26.8, 113.5, 116.7, 120.6, 121.8, 127.3, 128.4, 129.2, 130.6, 134.3, 135.1, 140.9, 148.9, 157.9. HRMS (ESI): calc'd for C26H26N4OSi [M+H]+: 438.1876, found: 438.1879.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08409820B2uspto-grants-2013_04