Hydrazine hydrate (1:1) → 2-[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetohydrazide

HRID 2405309Notes

Reaction equation

HRID 2405309 reaction equation
[CH:1]1([C:4]([N:6]2[CH2:10][CH2:9][C@@H:8]([CH2:11][C:12]([O:14]CC)=O)[CH2:7]2)=[O:5])[CH2:3][CH2:2]1.O.[NH2:18][NH2:19]>C(O)C.ClCCl>[CH:1]1([C:4]([N:6]2[CH2:10][CH2:9][C@@H:8]([CH2:11][C:12]([NH:18][NH2:19])=[O:14])[CH2:7]2)=[O:5])[CH2:3][CH2:2]1

Participants

5

Conditions

Temperature
80 °C

Procedure

In a round bottom flask equipped with reflux condenser, an orange solution of ethyl [(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetate (56.1 g, 249 mmol) in ethanol (356 mL) was treated with hydrazine monohydrate (242 mL, 4.98 mol). The resultant yellow solution was stirred at 80° C. (reflux) for 15 h. The reaction was cooled to room temperature and concentrated in vacuo. Ethanol (100 mL) was added and the reaction was concentrated (2×) to give a pale yellow clear oil. The oil was dissolved in dichloromethane (white solution observed), dried over MgSO4, concentrated in vacuo, and pumped under high vacuum overnight (16 h) to give the title compound as a clear pale yellow oil (249 mmol, quantitative). MS(ES)+ m/e 212.0 [M+H]+, 423.2 [2M+H]+.

Workup

  1. customIn a round bottom flask equipped
  2. temperaturewith reflux condenser
  3. temperature(reflux) for 15 h
  4. temperatureThe reaction was cooled to room temperature
  5. concentrationconcentrated in vacuo
  6. additionEthanol (100 mL) was added
  7. concentrationthe reaction was concentrated (2×)
  8. customto give a pale yellow clear oil
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. custompumped under high vacuum overnight (16 h)

Sources & evidence

ORD record
ord-51807bdb7ac8468e97007e2f0bc8877e
Source dataset
uspto-grants-2014_08
Patent number
US08802864B2

Reaction notes

Loading…