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Citric Acid → HCID 178483292、化合物

HRID 1480438
ノート
印刷プレビュー

反応式

HRID 1480438 の反応式
[C:1](Cl)(=[O:13])[O:2][CH2:3][C:4]1[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[C:6]([Cl:12])[CH:5]=1.[CH3:15][N:16]([CH2:24][CH2:25][CH:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1)[C:17]([C:19]1[N:20]=[N:21][NH:22][CH:23]=1)=[O:18].C(=O)(O)[O-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C(Cl)Cl>[CH3:15][N:16]([CH2:24][CH2:25][CH:26]1[CH2:27][CH2:28][N:29]([C:1]([O:2][CH2:3][C:4]2[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[C:6]([Cl:12])[CH:5]=2)=[O:13])[CH2:30][CH2:31]1)[C:17]([C:19]1[N:20]=[N:21][NH:22][CH:23]=1)=[O:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 311Citric AcidHCID 516892Sodium BicarbonateHCID 86722663HCID 86722663、化合物HCID 178483276HCID 178483276、化合物

生成物 1

HCID 178483292HCID 178483292、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 3-chloro-5-cyanobenzyl carbonochloridate (step 4) (65.5 mg, 0.285 mmol) and N-methyl-N-(2-(piperidin-4-yl)ethyl)-1H-1,2,3-triazole-4-carboxamide (step 3) (78 mg, 0.285 mmol) in DCM (5 mL) was added saturated aqueous sodium bicarbonate solution (5 mL, 0.285 mmol), and the mixture stirred vigorously for 16 hrs. The resulting mixture was acidified with 10% citric acid solution and the organic portion was separated, dried (MgSO4) and concentrated under reduced pressure. The residue was dissolved in DCM and applied to a 12 g silica cartridge eluting with 0-100% EtOAc/iso-hexane. The product fractions were combined and concentrated to give a gum. This was further purified by UV triggered HPLC, to give 3-chloro-5-cyanobenzyl 4-(2-(N-methyl-1H-1,2,3-triazole-4-carboxamido)ethyl)piperidine-1-carboxylate as a gum;

後処理

  1. customthe organic portion was separated
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe residue was dissolved in DCM
  5. washeluting with 0-100% EtOAc/iso-hexane
  6. concentrationconcentrated
  7. customto give a gum
  8. customThis was further purified by UV

出典と根拠

ORDレコード
ord-90db1c2ae3004b14a29bb500e8919bcb
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409895B2

反応ノート

読み込み中…

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