Formamide → HCID 57907619, compound

HRID 1888201Notes

Reaction equation

HRID 1888201 reaction equation
[NH2:1][N:2]1[C@H:6]([CH2:7][O:8][C:9]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:5][CH2:4][C:3]1=O.[CH:29]([NH2:31])=O>CN(C=O)C.C(OCC)(=O)C.[Cl-].[Zn+2].[Cl-]>[C:9]([O:8][CH2:7][C@H:6]1[N:2]2[N:1]=[CH:29][N:31]=[C:3]2[CH2:4][CH2:5]1)([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

6

Reactant 2

HCID 713FormamideHCID 57907607HCID 57907607, compound

Product 1

HCID 57907619HCID 57907619, compoundYield 49%

Reagents, catalysts & solvents 3

HCID 3007855ZincchlorideCatalystHCID 6228DimethylformamideSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
160 °C

Procedure

To a stirred solution of 0.540 g (1.45 mmol) of (5S)-1-amino-5-[(trityloxy)methyl]pyrrolidin-2-one from step A in 5 mL of anhydrous DMF was added 0.327 g (7.25 mmol) of formamide followed by 0.050 g (036 mmol) of zinc(II)chloride. The resulting mixture was heated to 160° C. for 48 h, cooled to ambient temperature and diluted with 25 mL of ethyl acetate. The solution was washed sequentially with an aqueous sodium bicarbonate solution, water and then brine and the organic layer dried over magnesium sulfate. The mixture was then filtered, evaporated to dryness in vacuo and purified by silica gel chromatography eluting with a 0-100% ethyl acetatae in hexanes gradient to afford the title compound (0.27 g, 49%). LC-MS: m/z (ES) 382 (MH)+.

Workup

  1. temperaturecooled to ambient temperature
  2. washThe solution was washed sequentially with an aqueous sodium bicarbonate solution, water
  3. dry with materialbrine and the organic layer dried over magnesium sulfate
  4. filtrationThe mixture was then filtered
  5. customevaporated to dryness in vacuo
  6. custompurified by silica gel chromatography
  7. washeluting with a 0-100% ethyl acetatae in hexanes gradient

Sources & evidence

ORD record
ord-6d1631a5ceab4eefb6fed79cc60f6990
Source dataset
uspto-grants-2013_08
Patent number
US08501786B2

Reaction notes

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