Acetic Acid → Octanedioic acid adamantan-1-ylamide hydroxyamide

HRID 1786743Notes

Reaction equation

HRID 1786743 reaction equation
Cl.[NH2:2][OH:3].[Na].C[O:6][C:7](=O)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14](=[O:26])[NH:15][C:16]12[CH2:25][CH:20]3[CH2:21][CH:22]([CH2:24][CH:18]([CH2:19]3)[CH2:17]1)[CH2:23]2.C(O)(=O)C>CO.O.C1C=CC2C(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)OC(=O)C=2C=1>[OH:3][NH:2][C:7](=[O:6])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([NH:15][C:16]12[CH2:25][CH:20]3[CH2:21][CH:22]([CH2:24][CH:18]([CH2:19]3)[CH2:17]1)[CH2:23]2)=[O:26]

Participants

8

Reactant 4

HCID 176Acetic AcidHCID 443297Hydroxyamine hydrochlorideHCID 5360545Sodium2×HCID 67006503HCID 67006503, compound

Product 1

HCID 53325741Octanedioic acid adamantan-1-ylamide hydroxyamideYield 68%

Reagents, catalysts & solvents 3

HCID 4764PhenolphthaleinCatalystHCID 887MethanolSolvent4×HCID 962WaterSolvent

Procedure

To a first solution of hydroxylamine hydrochloride (66 mg, 0.950 mmol) and phenolphthalein (0.5 mg) in methanol (3 mL), was added dropwise a second solution of sodium metal (33 mg, 1.435 mmol) in methanol (3 mL) via additional funnel until a pink endpoint was reached and precipitate appeared. To the reaction mixture was added a solution of 7-(adamantan-1-yl-carbamoyl)-heptanoic acid methyl ester (152 mg, 0.474 mmol) in methanol (4 mL) was added, followed by the remainder of the second solution of sodium metal in methanol. The resulting reaction was allowed to stir for 24 hours, then the reaction mixture was diluted with water (15 mL), followed by glacial acetic acid (0.2 mL) with stirring. The resulting precipitate was suction filtered and rinsed using water, then dried at room temperature under vacuum to provide a crude residue which was purified by recrystallization from dichloromethane/hexane to provide Compound 17 (104 mg, 68% yield). 1H NMR (300MHz, CD3OD) δ 7.31 (br s, 1H), 2.09(t, J=7.5 Hz, 2H), 2.08-1.98 (m, 11H), 1.71 (m, 6H), 1.59 (m, 4H), 1.33 (m, 4H). 13C NMR (75 MHz, CD3OD) δ 175.7, 173.1, 52.8, 42.5, 38.0, 37.7, 33.9, 31.1, 30.00, 29.96, 27.2, 26.8.

Workup

  1. additionwas added
  2. customThe resulting reaction
  3. stirringwith stirring
  4. filtrationfiltered
  5. washrinsed
  6. customdried at room temperature under vacuum
  7. customto provide a crude residue which
  8. customwas purified by recrystallization from dichloromethane/hexane

Sources & evidence

ORD record
ord-410a56935e554501b6be0dc88cc96e44
Source dataset
uspto-grants-2009_03
Patent number
US07507828B2

Reaction notes

Loading…