تفاعل #1077583

ord-60727ee7a3c943a588aa0a33438c1b4e

معادلة التفاعل

C[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C
N-tert-butoxycarbonyl-N-methyl-L-alanine
C[C@@H](C(=O)NCCCC(c1ccc(F)cc1)c1ccc(F)cc1)N(C)C(=O)OC(C)(C)C
(S){1-[4,4-Bis-(4-fluoro-phenyl)-butylcarbamoyl]-ethyl}-methyl-carbamic acid tert-butyl ester
CN[C@H](C)C(=O)NCCCC(c1ccc(F)cc1)c1ccc(F)cc1
(R)-N-[4,4-Bis-(4-fluoro-phenyl)-butyl]-2-methylamino-propionamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

(R)-N-[4,4-Bis-(4-fluoro-phenyl)-butyl]-2-methylamino-propionamide was prepared in accordance with the methods of Example 12, except that: N-tert-butoxycarbonyl-N-methyl-L-alanine was used instead of N-tert-butoxycarbonyl-N-methyl-L-leucine in Step A, and (S){1-[4,4-Bis-(4-fluoro-phenyl)-butylcarbamoyl]-ethyl}-methyl-carbamic acid tert-butyl ester was used instead of (S){1-[4,4-bis-(4-fluoro-phenyl)-butylcarbamoyl]-3-methyl-butyl}-methyl-carbamic acid tert-butyl ester in Step B. MS: 347 (M+1 for C20H24N2F2O1); an oil; Rf 0.3 (5% MeOH/CH2Cl2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06458781B1uspto-grants-2002_10