Benzocaine → Ethyl 4-(((2-acetamido-4-oxo-3,4-dihydropteridin-6-yl)methyl)amino)benzoate

HRID 372538ノート

反応式

HRID 372538 の反応式
CN(C)C=O.[C:6]([NH:9][C:10]1[N:19]=[C:18]([OH:20])[C:17]2[C:12](=[N:13][CH:14]=[C:15]([CH:21]=O)[N:16]=2)[N:11]=1)(=[O:8])[CH3:7].[NH2:23][C:24]1[CH:34]=[CH:33][C:27]([C:28]([O:30][CH2:31][CH3:32])=[O:29])=[CH:26][CH:25]=1.B.CNC>C(O)(=O)C>[C:6]([NH:9][C:10]1[NH:19][C:18](=[O:20])[C:17]2[C:12](=[N:13][CH:14]=[C:15]([N:16]=2)[CH2:21][NH:23][C:24]2[CH:25]=[CH:26][C:27]([C:28]([O:30][CH2:31][CH3:32])=[O:29])=[CH:33][CH:34]=2)[N:11]=1)(=[O:8])[CH3:7]

参加物

6

反応物 4

HCID 2337BenzocaineHCID 6228DimethylformamideHCID 6330borane;N-methylmethanamineHCID 178474471HCID 178474471、化合物

生成物 1

HCID 136354639Ethyl 4-(((2-acetamido-4-oxo-3,4-dihydropteridin-6-yl)methyl)amino)benzoate

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

実験手順

A mixture of 3.07 g (10 m ole) of the dimethylformamide solvate of 2-acetamido-4-hydroxypteridine-6-aldehyde, 3.30 g (20 mmole) of ethyl p-aminobenzoate and 50 ml of glacial acetic acid is stirred at ambient temperature for 30 minutes. To the resulting suspension is added dropwise 1.00 g of dimethylamine borane in 15 ml of acetic acid. The mixture is stirred for an additional 20 minutes, heated to 60° C for 10 minutes and cooled to 25° C. The precipitate is collected by filtration, washed with acetic acid and ether and then dried. The crude product is crystallized from 50 ml of dimethylformamide, with dilution by 20 ml ether, to yield ethyl N2 -acetylpteroate.

後処理

  1. stirringThe mixture is stirred for an additional 20 minutes
  2. temperatureheated to 60° C for 10 minutes
  3. temperaturecooled to 25° C
  4. filtrationThe precipitate is collected by filtration
  5. washwashed with acetic acid and ether
  6. customdried
  7. customThe crude product is crystallized from 50 ml of dimethylformamide, with dilution by 20 ml ether

出典と根拠

ORDレコード
ord-eb2c40b9d714422cb3235db0e0126dba
出典データセット
uspto-grants-1978_05
特許番号
US04091087

反応ノート

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