Triethylamine → HCID 136047358, compound

HRID 714501Notes

Reaction equation

HRID 714501 reaction equation
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:24])[C:7]([C:16]3[CH:23]=[CH:22][C:19]([C:20]#[N:21])=[CH:18][CH:17]=3)=[C:8]([C:12]([F:15])([F:14])[F:13])[O:9]2)=[CH:4][CH:3]=1.Cl.N[OH:27].C(N(CC)CC)C.C1N=CN([C:40]([N:42]2C=NC=C2)=[O:41])C=1>C(O)C>[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:24])[C:7]([C:16]3[CH:23]=[CH:22][C:19]([C:20]4[NH:42][C:40](=[O:27])[O:41][N:21]=4)=[CH:18][CH:17]=3)=[C:8]([C:12]([F:15])([F:13])[F:14])[O:9]2)=[CH:4][CH:3]=1

Participants

6

Procedure

Synthesis: To a solution of 4-(7-hydroxy-4-oxo-2-(trifluoromethyl)-4H-chromen-3-yl)benzonitrile (see Example 1, step 1 for synthesis) (200 mg, 0.60 mmol) and hydroxylamine hydrochloride (218 mg, 3.13 mmol) in absolute ethanol (2 ml) was added dropwise triethylamine (0.7 ml). The resulting mixture was heated to reflux for 5 hours. The volatiles were evaporated and the residue was dissolved in anhydrous THF (2 ml). CDI (296 mg, 1.83 mmol) was added and the suspension was heated to reflux overnight. The volatiles were evaporated and the residue was purified by prep-TLC (pure EtOAc) and prep-HPLC to afford desired product in Example 9 (35 mg, 15%) as a white solid.

Workup

  1. customSynthesis
  2. temperatureThe resulting mixture was heated
  3. temperatureto reflux for 5 hours
  4. customThe volatiles were evaporated
  5. dissolutionthe residue was dissolved in anhydrous THF (2 ml)
  6. temperaturethe suspension was heated
  7. temperatureto reflux overnight
  8. customThe volatiles were evaporated
  9. customthe residue was purified by prep-TLC (pure EtOAc)

Sources & evidence

ORD record
ord-243c369ae004402484968bd859454f7d
Source dataset
uspto-grants-2015_11
Patent number
US09187447B2

Reaction notes

Loading…