HCID 66676719, compound → HCID 21113031, compound

HRID 2242263Notes

Reaction equation

HRID 2242263 reaction equation
C([O:5][C:6](=[O:28])[CH2:7][N:8]([C:11]([O:13][CH2:14][CH:15]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:21]2[C:16]1=[CH:17][CH:18]=[CH:19][CH:20]=2)=[O:12])[NH:9][CH3:10])(C)(C)C>Cl>[C:11]([N:8]([CH2:7][C:6]([OH:28])=[O:5])[NH:9][CH3:10])([O:13][CH2:14][CH:15]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:21]2[C:16]1=[CH:17][CH:18]=[CH:19][CH:20]=2)=[O:12]

Participants

3

Reactant 1

HCID 66676719HCID 66676719, compound

Product 1

HCID 21113031HCID 21113031, compoundYield 72%

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

1 L, two-neck, round-bottomed-flask was fitted with a glass stopper and reflux condenser connected to a calcium tube. (N-Fmoc-N′-methyl-hydrazino)-acetic acid t-butyl ester (20 g, 52 mmol) was added. A solution of HCl (150 mL, 4 M solution in dioxane) was added slowly with vigorous stirring in an ice water bath. The reaction mixture was stirred at RT over 1 day. The solution was concentrated completely under reduced pressure at 40° C. A saturated aq. NaHCO3 solution (100 mL) was added and the aqueous layer was washed with diethyl ether (100 mL). Conc. HCl was added dropwise slowly at 0° C. (pH 2-3). The mixture was extracted and the organic layer was retained (500 mL, MC). The solution was dried with sodium sulfate and evaporated in vacuo. The residue was purified by recrystallization with n-hexane and ethyl acetate to give (N-Fmoc-N′-methyl-hydrazino)-acetic acid (12 g, 72%). 1H-NMR (DMSO-d6) δ 12.38 (s, 1H), 8.56 (b, 1H), 7.89˜7.86 (d, J=9 Hz, 2H,), 7.70˜7.67 (d, J=9 Hz, 2H,), 7.43˜7.29 (m, 4H), 4.29˜4.27 (d, J=6 Hz, 2H), 4.25˜4.20 (t, J=6 Hz, 1H), 3.47 (s, 2H), 2.56 (s, 3H).

Workup

  1. custom1 L, two-neck, round-bottomed-flask was fitted with a glass stopper
  2. temperaturereflux condenser
  3. customconnected to a calcium tube
  4. stirringThe reaction mixture was stirred at RT over 1 day
  5. concentrationThe solution was concentrated completely under reduced pressure at 40° C
  6. additionA saturated aq. NaHCO3 solution (100 mL) was added
  7. washthe aqueous layer was washed with diethyl ether (100 mL)
  8. additionConc. HCl was added dropwise slowly at 0° C. (pH 2-3)
  9. extractionThe mixture was extracted
  10. dry with materialThe solution was dried with sodium sulfate
  11. customevaporated in vacuo
  12. customThe residue was purified by recrystallization with n-hexane and ethyl acetate

Sources & evidence

ORD record
ord-c44c6c8f96634bfaa871b4c7a730b96c
Source dataset
uspto-grants-2010_03
Patent number
US07671054B1

Reaction notes

Loading…