Sodium bis(trimethylsilyl)amide → 3-Bromo-6-chloro-9H-dipyrido[2,3-b;4',3'-d]pyrrole

HRID 1505864Notes

Reaction equation

HRID 1505864 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:14]=[C:13]([Cl:15])[N:12]=[CH:11][C:10]=2[NH2:16])[C:5](F)=[N:6][CH:7]=1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+]>C1COCC1>[Br:1][C:2]1[CH:7]=[N:6][C:5]2[NH:16][C:10]3[CH:11]=[N:12][C:13]([Cl:15])=[CH:14][C:9]=3[C:4]=2[CH:3]=1

Participants

4

Procedure

A solution of 5-bromo-6′-chloro-2-fluoro-[3,4]bipyridinyl-3′-ylamine (2.21 g, 7.32 mmol) in THF (124 mL) was added dropwise over 10 minutes to sodium bis-(trimethylsilyl)amide (1N solution in THF, 14.6 mL, 14.6 mmol). The reaction mixture was stirred for 1 h at ambient temperature and then quenched by the addition of water (2 mL). The resultant brown solution was partitioned between ethyl acetate (75 mL) and brine (50 mL). An off-white solid precipitated and was collected by filtration to afford the title compound as a grey solid (1.01 g, 49%). 1H NMR (DMSO-D5, 300 MHz): 9.01 (d, J=2.3 Hz, 1H), 8.73 (s, 1H), 8.70 (d, J=2.3 Hz, 1H), 8.35 (s, 1H). LCMS (Method B): RT=3.33 min, M+H+=284.

Workup

  1. customquenched by the addition of water (2 mL)
  2. customThe resultant brown solution was partitioned between ethyl acetate (75 mL) and brine (50 mL)
  3. customAn off-white solid precipitated
  4. filtrationwas collected by filtration

Sources & evidence

ORD record
ord-040eaeb8b9f34c3485778d05b4282a4c
Source dataset
uspto-grants-2015_12
Patent number
US09216980B2

Reaction notes

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