ethyl N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamate → 1-[N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamoyl]-2-[N-(2,2,6,6-tetramethyl-4-piperidinyl)succinamoyl]hydrazine

HRID 1608863ノート

反応式

HRID 1608863 の反応式
[CH3:1][C:2]1([CH3:18])[CH2:7][CH:6]([NH:8][C:9](=[O:15])[C:10]([O:12]CC)=O)[CH2:5][C:4]([CH3:17])([CH3:16])[NH:3]1.[CH3:19][C:20]1([CH3:37])[CH2:25][CH:24]([NH:26][C:27](=[O:34])[CH2:28][CH2:29][C:30]([NH:32][NH2:33])=[O:31])[CH2:23][C:22]([CH3:36])([CH3:35])[NH:21]1>CO>[CH3:18][C:2]1([CH3:1])[CH2:7][CH:6]([NH:8][C:9](=[O:15])[C:10]([NH:33][NH:32][C:30](=[O:31])[CH2:29][CH2:28][C:27]([NH:26][CH:24]2[CH2:23][C:22]([CH3:35])([CH3:36])[NH:21][C:20]([CH3:37])([CH3:19])[CH2:25]2)=[O:34])=[O:12])[CH2:5][C:4]([CH3:16])([CH3:17])[NH:3]1

参加物

4

反応物 2

HCID 11118680ethyl N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamateHCID 14745323N-(2,2,6,6-tetramethyl-4-piperidinyl)-N'-aminosuccinamide

生成物 1

HCID 200857791-[N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamoyl]-2-[N-(2,2,6,6-tetramethyl-4-piperidinyl)succinamoyl]hydrazine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

Into a 3-necked 50 ml flask was introduced a 60.9% solution of ethyl N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamate in methanol (4.27 g, 0.01 mole), N-(2,2,6,6-tetramethyl-4-piperidinyl)-N'-aminosuccinamide (2.7 g, 0.01 mole) and 25 ml of anhydrous methanol. The flask was equipped with a thermometer, a magnetic stirrer and a Dean Stark trap with a reflux condenser. The reaction mixture was heated to reflux for 1/2 hour. Liquid chromatography of the reaction mixture indicated that the starting materials had essentially disappeared and there was one new peak corresponding to the product. The reaction mixture was filtered hot to remove some insoluble material. The filtrate was stripped to dryness on a rotatary evaporator under reduced pressure. The residue was scraped out of the flask and pulverized into a white powder with a mortar and pestle. The white powder was air dried on a watch glass overnight. The product weighed 1.0 grams and had a melting range of 130°-135° C. An infrared scan (nujol mull) of the product contained a strong carbonyl band at 1655 cm-1 and two moderate carbonyl bands at 1575 and 1495 cm-1.

後処理

  1. customThe flask was equipped with a thermometer, a magnetic stirrer
  2. temperatureThe reaction mixture was heated
  3. temperatureto reflux for 1/2 hour
  4. filtrationThe reaction mixture was filtered hot
  5. customto remove some insoluble material
  6. customThe filtrate was stripped to dryness on a rotatary evaporator under reduced pressure
  7. customdried on a watch glass overnight

出典と根拠

ORDレコード
ord-0f316ab12e97482eadb8df173e9270b4
出典データセット
uspto-grants-1995_03
特許番号
US05397821

反応ノート

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