تفاعل #838933

ord-7f5857906a5c4b5facf5ffce9d697e85

معادلة التفاعل

C[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C
N-Boc-N-methyl-L-alanine
CN1CCOCC1
N-methylmorpholine
C[C@H](N)C(=O)OCc1ccccc1.Cl
L-alanine benzyl ester hydrochloride
On1nnc2ccccc21
HOBt
ClCCCl
EDC
C[C@H](NC(=O)[C@H](C)N(C)C(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Benzyl (S)-2-[(S)-2-(tert-butoxycarbonyl-methyl-amino)-propanoylamino]-propionate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted
  2. 2
    workup.STIRRINGwith shaking
  3. 3
    استخلاصThe aqueous phase is extracted twice with toluene
  4. 4
    تجفيفthe combined organic phases are dried over sodium sulfate
  5. 5
    تركيزconcentrated to dryness
  6. 6
    ترشيحafter filtration
  7. 7
    أخرىThe product is purified chromatographically by silica gel chromatography on about 1500 ml of silica gel
  8. 8
    أخرى7.9 g (97% of th.) of the product are obtained

الإجراء التجريبي

4.81 g (22.3 mmol) of L-alanine benzyl ester hydrochloride, 3.32 g (24.6 mmol) of HOBt and 4.92 g (25.7 mmol) of EDC are introduced into 10 ml of anhydrous dimethylformamide under argon. At 0° C., 4.54 g (22.3 mmol) of N-Boc-N-methyl-L-alanine and 14.7 ml (133.9 mmol) of N-methylmorpholine are added, and the reaction mixture is stirred overnight with slow warming to RT. The reaction solution is treated with water and toluene and extracted with shaking. The aqueous phase is extracted twice with toluene, and the combined organic phases are dried over sodium sulfate and concentrated to dryness after filtration. The product is purified chromatographically by silica gel chromatography on about 1500 ml of silica gel using MeOH/dichloromethane 10/1. 7.9 g (97% of th.) of the product are obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07405201B2uspto-grants-2008_07