1-Methylpyrrolidine-2-methylamine → N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamide

HRID 127407

Reaction equation

HRID 127407 reaction equation
CO[C:3]([C:5]1[C:14]2[O:13][CH2:12][CH2:11][O:10][C:9]=2[CH:8]=[C:7](S(=O)(=O)NC)[CH:6]=1)=[O:4].[CH3:20][N:21]1[CH2:25][CH2:24][CH2:23][CH:22]1[CH2:26][NH2:27]>C(O)(=O)C.O>[CH3:20][N:21]1[CH2:25][CH2:24][CH2:23][CH:22]1[CH2:26][NH:27][C:3]([C:5]1[C:14]2[O:13][CH2:12][CH2:11][O:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:4]

Participants

5

Reactant 2

HCID 1173001-Methylpyrrolidine-2-methylamineHCID 54343297Methyl-7-methylsulfamoyl-1,4-benzodioxane-5-carboxylate

Product 1

HCID 53775438N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamideYield 112%

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolventHCID 962WaterSolvent2×

Procedure

169 g of methyl-7-methylsulfamoyl-1,4-benzodioxane-5-carboxylate, 53 ml of water and 81 g of 1-methyl-2-aminomethylpyrrolidine were introduced into a balloon flask provided with a reflux condenser. The mixture was heated on a water bath until a test sample was totally soluble in dilute acids. The resulting crystals were dissolved in a solution of 50 ml of acetic acid in 1,250 ml of water and then the solution was filtered over carbon black and the base was reprecipitated by the addition of 100 ml of 20% ammonia. The crystals were dried off, washed with water and dried. 182 g of N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamide was produced (M.P.: 189°-190° C.; yield: 83.6%).

Workup

  1. customprovided with a reflux condenser
  2. temperatureThe mixture was heated on a water bath until a test sample
  3. filtrationthe solution was filtered over carbon black
  4. customthe base was reprecipitated by the addition of 100 ml of 20% ammonia
  5. customThe crystals were dried off
  6. washwashed with water
  7. customdried

Sources & evidence

ORD record
ord-52d36f660dca4f7a94c7961311a582bd
Source dataset
uspto-grants-1981_03
Patent number
US04255580

Linked notes

Loading…