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Hydrochloric Acid → (2S,4S)-4-Fluoropyrrolidine-2-carboxamide

HRID 1430121
Notes
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Reaction equation

HRID 1430121 reaction equation
C(OC([N:8]1[CH2:12][C@@H:11]([F:13])[CH2:10][C@H:9]1[C:14](=[O:16])[NH2:15])=O)(C)(C)C.Cl>C(O)CCC>[F:13][C@@H:11]1[CH2:12][NH:8][C@H:9]([C:14]([NH2:15])=[O:16])[CH2:10]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 497605222-Methyl-2-propanyl (2S,4S)-2-carbamoyl-4-fluoro-1-pyrrolidinecarboxylate

Product 1

HCID 12066286(2S,4S)-4-Fluoropyrrolidine-2-carboxamide

Reagents, catalysts & solvents 1

HCID 2631-ButanolSolvent

Conditions

Temperature
50 °C

Procedure

A mixture of (2S,4S)-2-carbamoyl-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester (1.0 g), conc. Hydrochoric acid (0.6 ml) and 1-butanol (10 ml) is heated for 48 hours at 50° C. The reaction mixture is evaporated and partitioned dichloromethane and aqueous sodium bicarbonate, the dichloromethane layers are dried over sodium sulphate and evaporated. A solution of 7M ammonia in methanol (10 ml) is added to the residue and the mixture is stood for 60 hours at room temperature in a sealed vessel. Evaporation and trituration with ethanol gives the title compound as a white solid.

Workup

  1. customThe reaction mixture is evaporated
  2. custompartitioned dichloromethane and aqueous sodium bicarbonate
  3. dry with materialthe dichloromethane layers are dried over sodium sulphate
  4. customevaporated
  5. additionA solution of 7M ammonia in methanol (10 ml) is added to the residue
  6. customEvaporation and trituration with ethanol

Sources & evidence

ORD record
ord-85643e7558e241e58340ea2fdf0a5e44
Source dataset
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08940771B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes