Methylamine → N-[N-(3,5-dichlorophenyl)-D,L-alanyl]-(S)-2-aminohexan (N-methyl)-amide

반응식

[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][CH:10]([C:12]([OH:14])=O)[CH3:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[CH3:15][NH:16][C:17](=O)[C@H:18]([CH2:20][CH2:21][CH2:22][CH3:23])[NH2:19].C(N[C@H](C(O)=O)CCCC)(OC(C)(C)C)=O.CN>>[Cl:8][C:6]1[CH:5]=[C:4]([NH:9][CH:10]([C:12]([NH:19][C@H:18]([CH2:20][CH2:21][CH2:22][CH3:23])[CH3:17])=[O:14])[CH3:11])[CH:3]=[C:2]([Cl:1])[CH:7]=1.[CH3:15][NH-:16]

참가 물질

반응물 4

HCID 6329Methylamine

HCID 2733747N-tert-Butoxycarbonyl-L-norleucine

HCID 15484844N-(3,5-dichlorophenyl)-D,L-alanine

HCID 18341173l-Norleucine n-methyl amide

생성물 1

HCID 131721932N-[N-(3,5-dichlorophenyl)-D,L-alanyl]-(S)-2-aminohexan (N-methyl)-amide

실험 절차

Following General Procedure D and using N-(3,5-dichlorophenyl)-D,L-alanine and L-norleucine N-methyl amide (prepared by coupling BOC-L-norleucine (Bachem) with methylamine (Aldrich) using General Procedure E, followed by removal of the BOC group using General Procedure F), the title compound was prepared. The reacticon was monitored by tlc (Rf=0.25 in 3% methanol/dichloromethane) and purification of this compound was by thin layer chromatography with 3% methanol/dichloromethane.