Acetic Acid → HCID 69085270, compound

HRID 1455159Notes

Reaction equation

HRID 1455159 reaction equation
[NH2:1][C@@H:2]([C:6]1[N:11]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:10](=[O:19])[C:9]([CH3:20])=[C:8]([CH3:21])[N:7]=1)[CH:3]([CH3:5])[CH3:4].[CH:22]1[N:23](CC=O)[CH:24]=[C:25]2[C:30]=1[CH:29]=[CH:28][CH:27]=[CH:26]2.[C:34]([OH:37])(=O)[CH3:35].C(O[BH-](OC(=O)C)OC(=O)C)(=[O:40])C.[Na+]>ClC(Cl)C.CCOC(C)=O.CCCCCC>[CH2:12]([N:11]1[C:10](=[O:19])[C:9]([CH3:20])=[C:8]([CH3:21])[N:7]=[C:6]1[C@H:2]([NH:1][CH2:30][CH2:22][N:23]1[C:34](=[O:37])[C:35]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24]1=[O:40])[CH:3]([CH3:4])[CH3:5])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Participants

7

Procedure

2-((R)-1-Amino-2-methyl-propyl)-3-benzyl-5,6-dimethyl-3-H-pyrimidin-4-one (0.500 g, 1.75 mMol) and 2H-isoindole-2-acetaldehyde [2913-97-5] (0.661 g, 3.50 mMol) were dissolved in dichloroethane (20 mL). Glacial acetic acid was added (0.400 mL, 0.70 mMol) followed by sodium triacetoxy borohydride (0.942 g, 4.40 mMol). The reaction stirred at room temperature under nitrogen for 3.5 h. The reaction was quenched with NaHCO3 (sat. Aq.) and extracted with EtOAc (3×). The organic layer was evaporated under reduced pressure and purified by flash chromatography. (EtOAc/hexane 50-95% gradient) to give the title compound 420 mg (0.92 mMol) MS (ES) m/e 459 (M+H)+.

Workup

  1. customThe reaction was quenched with NaHCO3 (sat. Aq.)
  2. extractionextracted with EtOAc (3×)
  3. customThe organic layer was evaporated under reduced pressure
  4. custompurified by flash chromatography

Sources & evidence

ORD record
ord-279a7164e0174028b847a24f36cecf71
Source dataset
uspto-grants-2009_01
Patent number
US07482343B2

Reaction notes

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