Hydrochloric Acid → ethyl N-((7-chloro-2,3-dihydro-2-methyl-4-benzofuranylhydrazono)cyanoacetyl)carbamate

HRID 344598Notes

Reaction equation

HRID 344598 reaction equation
[NH2:1][C:2]1[C:7]2[CH2:8][CH:9]([CH3:11])[O:10][C:6]=2[C:5]([Cl:12])=[CH:4][CH:3]=1.Cl.[N:14]([O-])=O.[Na+].[C:18]([CH2:20][C:21]([NH:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])=[O:22])#[N:19]>O.N1C=CC=CC=1>[Cl:12][C:5]1[C:6]2[O:10][CH:9]([CH3:11])[CH2:8][C:7]=2[C:2]([NH:1][N:14]=[C:20]([C:18]#[N:19])[C:21]([NH:23][C:24](=[O:25])[O:26][CH2:27][CH3:28])=[O:22])=[CH:3][CH:4]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 23112N-CyanoacetylethylcarbamateHCID 23668193Sodium NitriteHCID 536714607-Chloro-2-methyl-2,3-dihydrobenzofuran-4-amine

Product 1

HCID 86743513ethyl N-((7-chloro-2,3-dihydro-2-methyl-4-benzofuranylhydrazono)cyanoacetyl)carbamate

Reagents, catalysts & solvents 2

HCID 962WaterSolvent5×HCID 1049PyridineSolvent

Procedure

A mixture of 9.18 g of 32A, 10 mL of 12N hydrochloric acid and 10 mL of water was heated on a steam bath for 1 hour, then 10 mL of water was added and the mixture was stirred at room temperature overnight. Then 30 mL of water was added, the mixture was cooled to 0° C. and stirred while a solution of 3.45 g of sodium nitrite in 10 mL of water was added dropwise over 15 minutes, then was stirred for 1 hour at 0° C. The resulting mixture was added slowly to a stirred mixture of 7.8 g of N-cyanoacetylurethane, 35 mL of pyridine and 900 mL of water, at 0° C. The resulting mixture was stirred at 0° C. for 1.5 hours, and filtered. The collected solid phase was washed with water, dried under reduced pressure and recrystallized from acetone/petroleum ether to give ethyl N-((7-chloro-2,3-dihydro-2-methyl- 4-benzofuranylhydrazono)cyanoacetyl)carbamate (32B), as a solid, m.p.: 175°-177° C. (with decomposition).

Workup

  1. temperaturewas heated on a steam bath for 1 hour
  2. temperaturethe mixture was cooled to 0° C.
  3. additionwas added dropwise over 15 minutes
  4. stirringwas stirred for 1 hour at 0° C
  5. stirringThe resulting mixture was stirred at 0° C. for 1.5 hours
  6. filtrationfiltered
  7. washThe collected solid phase was washed with water
  8. customdried under reduced pressure
  9. customrecrystallized from acetone/petroleum ether

Sources & evidence

ORD record
ord-364e391402aa425398df2eac91397f2b
Source dataset
uspto-grants-1991_10
Patent number
US05053071

Reaction notes

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