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

HRID 525127Notes

Reaction equation

HRID 525127 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-411935610315439ba43f376c7f3fe5b8
Source dataset
uspto-grants-2016_05
Patent number
US09340529B2

Reaction notes

Loading…