Ethylamine → HCID 118366250, compound

HRID 59927Notes

Reaction equation

HRID 59927 reaction equation
[CH2:1]([NH2:3])[CH3:2].C(N(CC)CC)C.[Cl:11][C:12]1[N:17]=[CH:16][C:15]([C:18](Cl)=[O:19])=[CH:14][N:13]=1>ClCCl>[Cl:11][C:12]1[N:17]=[CH:16][C:15]([C:18]([NH:3][CH2:1][CH3:2])=[O:19])=[CH:14][N:13]=1

Participants

5

Conditions

Temperature
-15 °C

Procedure

A solution of ethylamine (4.26 g, 0.0946 mol) and triethylamine (28.7 g, 0.284 mol) in dichloromethane (75 mL), pre-cooled to −15 to −10° C., was added dropwise to a solution of 2-chloropyrimidine-5-carbonyl chloride (16.64 g, 0.0946 mmol) in dry dichloromethane (250 mL) at −15° C., then the reaction mixture was stirred at −15° C. for 1 hour. The reaction was quenched by the addition of a solution of concentrated hydrochloric acid (32.3 mL) in water (300 mL). The resulting mixture was stirred at room temperature for 1 hour. The layers were separated, and the aqueous phase was further extracted with dichloromethane (3×200 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated. The crude residue was purified via column chromatography to provide 2-chloro-N-ethylpyrimidine-5-carboxamide (12.75 g, 72%).

Workup

  1. customThe reaction was quenched by the addition of a solution of concentrated hydrochloric acid (32.3 mL) in water (300 mL)
  2. stirringThe resulting mixture was stirred at room temperature for 1 hour
  3. customThe layers were separated
  4. extractionthe aqueous phase was further extracted with dichloromethane (3×200 mL)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude residue was purified via column chromatography

Sources & evidence

ORD record
ord-d15a02b2f6664d06b7c52161a11b2319
Source dataset
uspto-grants-2016_09
Patent number
US09440949B2

Reaction notes

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