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Triethylamine → HCID 67089257、化合物

HRID 2075627
ノート
印刷プレビュー

反応式

HRID 2075627 の反応式
Cl.[NH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:22])[O:7][CH2:8][CH:9]1[C:21]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:15]2[C:10]1=[CH:11][CH:12]=[CH:13][CH:14]=2.[C:23](O)(=[O:31])[C@@H:24]([C@H:26]([C:28]([OH:30])=[O:29])[OH:27])[OH:25].C(N(CC)CC)C.O.ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C>CN(C)C=O.C(OCC)(=O)C>[CH:11]1[C:10]2[CH:9]([CH2:8][O:7][C:6]([NH:5][CH2:4][CH2:3][NH:2][C:23](=[O:31])[CH:24]([OH:25])[CH:26]([OH:27])[C:28]([OH:30])=[O:29])=[O:22])[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]=2[CH:14]=[CH:13][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 8471TriethylamineHCID 444305L-Tartaric acid2 回HCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 2818106(9H-fluoren-9-yl)methyl N-(2-aminoethyl)carbamate hydrochloride2 回

生成物 1

HCID 67089257
HCID 67089257、化合物
収率 42%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

9H-9-fluorenylmethyl N-(2-aminoethyl)carbamate hydrochloride (Compound 14; 5.00 g, 153.7 mmol) and L-(+)-tartaric acid (Compound 15; 5.89 g, 39.2 mmol) were dissolved by the addition of N,N-dimethylformamide (300 ml) and triethylamine (5.46 ml, 39.2 mmol). Next, 1-hydroxybenzotriazol hydrate (2.52 g, 16.5 mmol) was added, a solution of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (3.16 g, 16.5 mmol) in N,N-dimethylformamide (200 ml) was added drop by drop, and this was followed by overnight stirring at room temperature. This was concentrated under reduced pressure, the residue obtained was dissolved in ethyl acetate, and the organic phase was washed with a 2N aqueous solution of citric acid. Next, reverse extraction was conducted using aqueous sodium hydrogen carbonate, after which the water phase obtained was washed with ethyl acetate. Under ice cooling, the water phase was rendered acidic with a 2N aqueous solution of citric acid, after which it was extracted with ethyl acetate. The organic phase was washed with saturated brine, after which it was dried with sodium sulfate. After the solid was filtered and concentrated under reduced pressure, crystallization from methanol-diethyl ether was conducted to yield the desired N-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-ethyl]-2,3-dihydroxy-succinamic acid (2.72 g, 42%).

後処理

  1. concentrationThis was concentrated under reduced pressure
  2. customthe residue obtained
  3. washthe organic phase was washed with a 2N aqueous solution of citric acid
  4. extractionextraction
  5. customafter which the water phase obtained
  6. washwas washed with ethyl acetate
  7. extractionafter which it was extracted with ethyl acetate
  8. washThe organic phase was washed with saturated brine
  9. dry with materialafter which it was dried with sodium sulfate
  10. filtrationAfter the solid was filtered
  11. concentrationconcentrated under reduced pressure, crystallization from methanol-diethyl ether

出典と根拠

ORDレコード
ord-d15319ad9ec64f75a3e924d6ebd571c9
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07919653B2

反応ノート

読み込み中…

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