تفاعل #11695

ord-ca029937102741169ab21ba3db64bf5e

معادلة التفاعل

C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)c1ccccc1CN
(S)—N-t-butyloxycarbonyl(2-aminomethylphenyl)alanine
CN(C)C=O
N,N-dimethylformamide
On1nnc2cccnc21
1-hydroxy-7-azabenzotriazole
CCN=C=NCCCN(C)C.Cl
1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride
CC(C)(C)OC(=O)N[C@H]1Cc2ccccc2CNC1=O
(S)-4-(t-butyloxycarbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was removed under vacuum
  2. 2
    workup.DISSOLUTIONthe residue was dissolved ethyl acetate (100 mL)
  3. 3
    غسيلThis solution was washed sequentially with 1.0 M aqueous hydrochloric acid (50 mL twice), 1.0 M aqueous sodium hydroxide (50 mL), water (50 mL), and brine (50 mL)
  4. 4
    تجفيفdried over anhydrous sodium sulfate
  5. 5
    أخرىevaporated under vacuum

الإجراء التجريبي

A mixture of (S)—N-t-butyloxycarbonyl(2-aminomethylphenyl)alanine (353 mg), N,N-dimethylformamide (10 mL), dichloromethane (50 mL), 1-hydroxy-7-azabenzotriazole (252 mg), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (180 mg) was stirred at room temperature for 1 h. The solvent was removed under vacuum and the residue was dissolved ethyl acetate (100 mL). This solution was washed sequentially with 1.0 M aqueous hydrochloric acid (50 mL twice), 1.0 M aqueous sodium hydroxide (50 mL), water (50 mL), and brine (50 mL), dried over anhydrous sodium sulfate, and evaporated under vacuum to obtain (S)-4-(t-butyloxycarbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one (315 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07098235B2uspto-grants-2006_08