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Fmoc-Gly-OH → L-Phenylalanine

HRID 1441193
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HRID 1441193 반응식
[C:1]([N:18](C)[C@H:19]([C:27]([OH:29])=[O:28])[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O.C(N(C)[C@H](C(O)=O)CC(=O)OC(C)(C)C)(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O.[NH:62](C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)[C@H:63]([C:68]([OH:70])=[O:69])[CH2:64][CH2:65][CH2:66][CH3:67].[NH:88](C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)[C@H:89]([C:100]([OH:102])=[O:101])[CH2:90][C:91]1[C:99]2[C:94](=[CH:95][CH:96]=[CH:97][CH:98]=2)[NH:93][CH:92]=1.N(C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)CC(O)=O>>[NH2:18][C@H:19]([C:27]([OH:29])=[O:28])[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[NH:18]([CH3:1])[C@H:19]([C:27]([OH:29])=[O:28])[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[NH2:62][C@H:63]([C:68]([OH:70])=[O:69])[CH2:64][CH2:65][CH2:66][CH3:67].[NH2:88][C@H:89]([C:100]([OH:102])=[O:101])[CH2:90][C:91]1[C:99]2[C:94](=[CH:95][CH:96]=[CH:97][CH:98]=2)[NH:93][CH:92]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 93124Fmoc-Gly-OHHCID 978343Fmoc-L-tryptophanHCID 978356(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-phenylpropanoic acidHCID 7009636(2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acid2회HCID 7019716N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-alpha-methyl-L-aspartic acid beta-t-butyl ester

생성물 4

HCID 6140L-Phenylalanine
HCID 6305L-Tryptophan
HCID 21236Caprine
HCID 6951135N-Methylphenylalanine

실험 절차

By following essentially the procedure of Table 2 and sequentially coupling Fmoc-MePhe-OH, Fmoc-MeAsp(OtBu)-OH, Fmoc-Ahx-OH, Fmoc-Trp-OH, Fmoc-Gly-OH, Fmoc-Ahx-OH and Hpa-OSu, the title compound was prepared. Amino Acid analysis following acid decomposition gave MeAsp 1.01 (1), Gly 1.05 (1), MePhe 0.91 (1), Ahx 2.02 (2), Trp 0.84 (1), NH3 0.82. MS (FAB): m/e 909 (M-H)-.

출처 및 근거

ORD 기록
ord-0e70947c102c424092ae9d4f378d191a
출처 데이터셋
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05502164

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