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L-Serine → Z-Glu(OBzl)-Ser-OH

HRID 462928
ノート
印刷プレビュー

反応式

HRID 462928 の反応式
[NH:1]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[C@H:2]([C:15]([OH:17])=O)[CH2:3][CH2:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.ON1C(=O)CCC1=O.[NH2:36][C@H:37]([C:40]([OH:42])=[O:41])[CH2:38][OH:39].C(N(CC)CC)C>O1CCCC1.CN1CCOCC1.ClC(OCC(C)C)=O.O>[NH:1]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[C@H:2]([C:15]([NH:36][C@H:37]([C:40]([OH:42])=[O:41])[CH2:38][OH:39])=[O:17])[CH2:3][CH2:4][C:5](=[O:14])[O:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 5951L-SerineHCID 8471TriethylamineHCID 80170N-HydroxysuccinimideHCID 30498605-(Phenylmethyl) hydrogen N-((phenylmethoxy)carbonyl)-L-glutamate

生成物 1

HCID 13385129Z-Glu(OBzl)-Ser-OH収率 76.9%

試薬・触媒・溶媒 4

HCID 962Water
溶媒
HCID 79724-Methylmorpholine溶媒
HCID 8028Tetrahydrofuran溶媒2 回
HCID 62365Isobutyl chloroformate溶媒

反応条件

温度
-15 °C

実験手順

To a solution of Z-Glu(OBzl)OH (5.62 g, 15 m mole) (Hayakawa et al. Bull. Chem. Soc. Japan, 39: 391 (1966)) in tetrahydrofuran (20 ml), N-methylmorpholin (1.53 ml) and isobutyl chloroformate (1.98 ml) were added with stirring at -15° C. To this mixture a solution of HOSu (N-hydroxy-succinimide) (3.45 g) in tetrahydrofuran (10 ml) was added with stirring at -15° C. The mixture was stirred at -15° C. for 30 min., and at 0° C. for 30 min. To this mixture a solution of H-Ser-OH (3.15 g, 30 mmole) in H2O (15 ml) containing triethylamine (4.2 ml) was added with stirring at 0° C. The mixture was stirred at 0° C. for 2 hr. and at room temperature for 15 hr. After removal of the organic solvent, the residue was extracted with three portions of ethyl acetate, which were washed successively with 1N citric acid and sat. NaCl solution, and dried over Na2SO4. After evaporating the residue was solidified by addition of ether. Reprecipitation from methanol-ether to yield (I) (5.29 g, 76.9%), RfI 0.74 RfII 0.70, mp 104°-105° C. [α]D27 +5.7 (C=1.12 in methanol).

後処理

  1. stirringwith stirring at -15° C
  2. stirringThe mixture was stirred at -15° C. for 30 min.
  3. additionwas added
  4. stirringwith stirring at 0° C
  5. stirringThe mixture was stirred at 0° C. for 2 hr
  6. waitand at room temperature for 15 hr
  7. customAfter removal of the organic solvent
  8. extractionthe residue was extracted with three portions of ethyl acetate, which
  9. washwere washed successively with 1N citric acid and sat. NaCl solution
  10. dry with materialdried over Na2SO4
  11. customAfter evaporating the residue
  12. additionwas solidified by addition of ether
  13. customReprecipitation from methanol-ether

出典と根拠

ORDレコード
ord-759ebb41ab394f4cb105107fb97fa18c
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04518527

反応ノート

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