Hydrochloric Acid → HCID 66701197, compound

HRID 2062061Notes

Reaction equation

HRID 2062061 reaction equation
[F:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][CH:15]=2)=[C:4]([C:24](O)=[O:25])[CH:3]=1.ON1C2C=CC=CC=2N=N1.Cl.[CH3:38][O:39][C:40](=[O:45])[C:41]([CH3:44])([CH3:43])[NH2:42].C(N(C(C)C)CC)(C)C.Cl>O.CN(C=O)C.C(Cl)CCl>[CH3:38][O:39][C:40](=[O:45])[C:41]([NH:42][C:24]([C:4]1[CH:3]=[C:2]([F:1])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]=1[O:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][CH:15]=1)=[O:25])([CH3:44])[CH3:43]

Participants

9

Procedure

To 0.2 g of 4-fluoro-1-[4-(trifluoromethyl)benzyloxy]naphthalene-2-carboxylic acid, 158 mg of EDC, 104 mg of 1-hydroxybenzotriazole and 102 mg of 2,2-dimethylglycine methyl ester hydrochloride was added 5.3 ml of DMF followed by 0.29 ml of diisopropylethylamine. The mixture was stirred for 16 h at room temperature. The mixture was poured into cold water, acidified to pH 2-3 with 1M HCl, extracted with ethyl acetate, washed with water, brine, dried (sodium sulphate) filtered and concentrated to an oil. The material was flash chromatographed on silica gel eluting with ethyl acetate/heptanes to provide 0.207 g of 2-{[4-fluoro-1-(4-trifluoromethyl-benzyloxy)-naphthalene-2-carbonyl]-amino}-2-methyl-propionic acid methyl ester as a colorless oil.

Workup

  1. extractionextracted with ethyl acetate
  2. washwashed with water, brine
  3. dry with materialdried (sodium sulphate)
  4. filtrationfiltered
  5. concentrationconcentrated to an oil
  6. customchromatographed on silica gel eluting with ethyl acetate/heptanes

Sources & evidence

ORD record
ord-c3000591f06c4f7993c0416b63664459
Source dataset
uspto-grants-2012_10
Patent number
US08283479B2

Reaction notes

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