반응 #88591

ord-95acc7fd569241d6829c8f213154a520

반응 방정식

O=S([O-])S(=O)(=O)[O-].[Na+].[Na+]
sodium metabisulfite
ClI
iodine monochloride
Brc1cc2c(cn1)[nH]c1ncccc12
6-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole
CC(=O)[O-].[Na+]
sodium acetate
Brc1cc2c(cn1)[nH]c1ncc(I)cc12
title compound
수율 84.2%
Brc1cc2c(cn1)[nH]c1ncc(I)cc12
6-Bromo-3-iodo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole
수율 84.2%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The resultant precipitate was collected by filtration
  2. 2
    세척the solid was washed with water (50 mL) and diethyl ether (2×50 mL)
  3. 3
    기타then dried at 45° C. until constant weight

실험 절차

A solution of iodine monochloride (32.5 g, 200 mmol) in acetic acid (120 mL) was added portionwise over 2 h to a mixture of 6-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole (5.0 g, 20 mmol) and sodium acetate (18.2 g, 221 mmol) in acetic acid (120 mL) at 100° C. The reaction mixture was cooled to ambient temperature and poured into saturated sodium metabisulfite solution (20% w/w, 400 mL). The resultant precipitate was collected by filtration and the solid was washed with water (50 mL) and diethyl ether (2×50 mL) then dried at 45° C. until constant weight was achieved, to afford the title compound as a grey solid (6.3 g, 83%). 1H NMR (DMSO-D6, 300 MHz) 12.49 (s, 1H); 9.14 (d, J=2.1 Hz, 1H); 8.79 (d, J=2.1 Hz, 1H); 8.71 (s, 1H); 8.49 (s, 1H). LCMS (Method B): RT=3.40 min, M+H+=374/376.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09440976B2uspto-grants-2016_09