2-(Dimethylamino)acetyl chloride hydrochloride → 4-Ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-(2-dimethylaminoacetamido)benzene

HRID 1834803Notes

Reaction equation

HRID 1834803 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([S:8][CH2:9][CH3:10])[CH:5]=[CH:4][C:3]=1[NH:11][C:12]([NH:14][C:15]([O:17][CH3:18])=[O:16])=[S:13].Cl.[CH3:20][N:21]([CH3:26])[CH2:22][C:23](Cl)=[O:24]>CN(C)C=O.C(OCC)C>[CH2:9]([S:8][C:6]1[CH:5]=[CH:4][C:3]([NH:11][C:12]([NH:14][C:15]([O:17][CH3:18])=[O:16])=[S:13])=[C:2]([NH:1][C:23](=[O:24])[CH2:22][N:21]([CH3:26])[CH3:20])[CH:7]=1)[CH3:10]

Participants

5

Procedure

A stirred solution of 2-amino-4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)benzene (8.35 g) in dry dimethylformamide (60 ml) was treated at room temperature with N,N-dimethylglycyl chloride hydrochloride (5.53 g). The mixture was heated to 40°-50° C for 45 minutes, then cooled, and diluted with diethyl ether (900 ml). An oil precipitated which crystallised on standing. This solid was filtered off, washed with diethyl ether (100 ml), and suspended in a mixture of chloroform (100 ml) and water (100 ml). Sodium carbonate (3.5 g) was added and the mixture was stirred for 20 minutes. The chloroform layer was separated and the aqueous layer was extracted twice with chloroform (2 × 50 ml). The organic layers were combined, dried over magnesium sulphate and evaporated to dryness. The residual solid was recrystallised from isopropanol to give 4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-(2-dimethylaminoacetamido)benzene (8.5 g), m.p. 142° C (with decomposition).

Workup

  1. temperatureThe mixture was heated to 40°-50° C for 45 minutes
  2. temperaturecooled
  3. customAn oil precipitated which
  4. customcrystallised
  5. filtrationThis solid was filtered off
  6. washwashed with diethyl ether (100 ml)
  7. additionsuspended in a mixture of chloroform (100 ml) and water (100 ml)
  8. additionSodium carbonate (3.5 g) was added
  9. customThe chloroform layer was separated
  10. extractionthe aqueous layer was extracted twice with chloroform (2 × 50 ml)
  11. dry with materialdried over magnesium sulphate
  12. customevaporated to dryness
  13. customThe residual solid was recrystallised from isopropanol

Sources & evidence

ORD record
ord-d95974e17d564809b66b2a29da0d0765
Source dataset
uspto-grants-1978_01
Patent number
US04071528

Reaction notes

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