Triethylamine → HCID 59165834, compound

HRID 2420864Notes

Reaction equation

HRID 2420864 reaction equation
[Br:1][C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][CH:3]=1.CCN(CC)CC.[F:16][C:17]1([F:32])[O:21][C:20]2[CH:22]=[CH:23][C:24]([C:26]3([C:29](Cl)=[O:30])[CH2:28][CH2:27]3)=[CH:25][C:19]=2[O:18]1>ClCCl>[Br:1][C:2]1[N:7]=[C:6]([NH:8][C:29]([C:26]2([C:24]3[CH:23]=[CH:22][C:20]4[O:21][C:17]([F:32])([F:16])[O:18][C:19]=4[CH:25]=3)[CH2:28][CH2:27]2)=[O:30])[CH:5]=[CH:4][CH:3]=1

Participants

5

Procedure

To a solution of 6-bromopyridin-2-amine (660 mg, 3.8 mmol) and Et3N (1.1 mL, 7.7 mmol) in dichloromethane (5 mL) was added a solution of 1-(2,2-difluorobenzo-[d][1,3]dioxol-5-yl)cyclopropanecarbonyl chloride (1.0 g, 3.8 mmol) in dichloromethane (5 mL). The resulting reaction mixture was allowed to stir at room temperature for 18 hours. The reaction mixture was diluted with dichloromethane (5 mL) and was washed with 1 N aqueous HCl (1×10 mL) and saturated aqueous NaHCO3 (1×10 mL). The organics were dried over sodium sulfate and evaporated to dryness. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-70% ethyl acetate in hexane to yield N-(6-bromopyridin-2-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide (780 mg, 51%). 1H NMR (400 MHz, DMSO-d6) δ 9.46 (s, 1H), 8.01-7.99 (m, 1H), 7.75-7.71 (m, 1H), 7.54 (m, 1H), 7.41-7.39 (m, 1H), 7.36-7.30 (m, 2H), 1.52-1.49 (m, 2H), 1.20-1.17 (m, 2H). ESI-MS m/z calc. 396.0, found 397.3 (M+1)+. Retention time 2.12 minutes.

Workup

  1. customThe resulting reaction mixture
  2. washwas washed with 1 N aqueous HCl (1×10 mL) and saturated aqueous NaHCO3 (1×10 mL)
  3. dry with materialThe organics were dried over sodium sulfate
  4. customevaporated to dryness
  5. customThe resulting residue was purified by silica gel chromatography
  6. washeluting with a gradient of 0-70% ethyl acetate in hexane

Sources & evidence

ORD record
ord-7ca96a12b0af4c0d832acd2a3aebee53
Source dataset
uspto-grants-2011_06
Patent number
US07956052B2

Reaction notes

Loading…