Formamide → HCID 178461168, compound

HRID 1806064Notes

Reaction equation

HRID 1806064 reaction equation
[NH2:1][C:2]1[CH2:6][CH2:5][C@@H:4]([CH3:7])[C:3]=1[C:8]([O:10]CC)=O.C([O-])=O.[NH4+].[CH:17]([NH2:19])=O>C1(C)C=CC=CC=1>[CH3:7][C@H:4]1[C:3]2[C:8]([OH:10])=[N:19][CH:17]=[N:1][C:2]=2[CH2:6][CH2:5]1

Participants

5

Conditions

Temperature
150 °C

Procedure

A 2 L 3-neck round bottom flask equipped with a condenser, internal temperature probe, was charged with (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (185 g, 1093 mmol) and ammonium formate (103.4 g, 1640 mmol) in formamide (400 mL) and toluene (200 mL). The reaction was heated to an internal temperature of 150° C. and stirred for 36 hours. The reaction was cooled and transferred to a 2 L single next flask and excess formamide was removed by high vacuum distillation. The resulting oil was dissolved in CH2Cl2 and washed with brine. The combined aqueous layers were extracted with CH2Cl2. The combined organic layers were dried over sodium sulfate, filtered and concentrated to give the crude product as a brown semi solid which was taken into the next step without any further purification.

Workup

  1. customA 2 L 3-neck round bottom flask equipped with a condenser
  2. temperatureThe reaction was cooled
  3. customtransferred to a 2 L single next flask
  4. customexcess formamide was removed by high vacuum distillation
  5. dissolutionThe resulting oil was dissolved in CH2Cl2
  6. washwashed with brine
  7. extractionThe combined aqueous layers were extracted with CH2Cl2
  8. dry with materialThe combined organic layers were dried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-1618e8597c404ef3b2241f2b1c9cd16a
Source dataset
uspto-grants-2013_01
Patent number
US08354540B2

Reaction notes

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