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

HRID 2052626

반응식

HRID 2052626 반응식
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]

참가 물질

5

반응물 2

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

생성물 1

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

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

실험 절차

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% 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%).

후처리

  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% ml of 20% ammonia
  5. customThe crystals were dried off
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-c4426c0ad46c4a8da6fb6c852e4769b7
출처 데이터셋
uspto-grants-1980_01
특허 번호
US04186135

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