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N2 [(1,1-dimethylethoxycarbonyl]-N6-[(phenylmethoxy)carbonyl]-(R)-6-[(phenylmethoxy)carbonyl]-L-lysyl]-D-Alanine Phenylmethyl Ester → HCID 67798175, 화합물

HRID 2258045
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HRID 2258045 반응식
N#N.[C:3]1([CH2:9][O:10][C:11](=[O:51])[C@@H:12]([CH3:50])[NH:13][C:14](=[O:49])[C@@H:15]([CH2:24][CH2:25][CH2:26][CH:27]([C:39]([O:41][CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)=[O:40])[NH:28][C:29]([O:31][CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)=[O:30])[NH:16]C(OC(C)(C)C)=O)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)(C(F)(F)F)=O>[C:3]1([CH2:9][O:10][C:11](=[O:51])[C@@H:12]([CH3:50])[NH:13][C:14](=[O:49])[C@@H:15]([CH2:24][CH2:25][CH2:26][CH:27]([C:39]([O:41][CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)=[O:40])[NH:28][C:29]([O:31][CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)=[O:30])[NH2:16])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86751171N2 [(1,1-dimethylethoxycarbonyl]-N6-[(phenylmethoxy)carbonyl]-(R)-6-[(phenylmethoxy)carbonyl]-L-lysyl]-D-Alanine Phenylmethyl Ester

생성물 1

HCID 67798175HCID 67798175, 화합물수율 105.6%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 40b (251 mg, 0.37 mmol) in TFA (870 μl) is stirred for 30 min at 0° C. The TFA is removed and the oil is taken up in EtOAc and washed with saturated NaHCO3 solution. Drying and removal of the solvent gives 3b (225 mg, slight excess) which is used in subsequent reactions without further handling: NMR δ 1.39 (d, 3 H) and 1.20-1.70 (overlapping m, 4 H), 1.82 (br s, 2 H), 3.23 (br s, variable, 2 H), 3.33 (br s, 1 H), 4.39 (m, 1 H), 4.47 (apparent quintet, 1 H), 5.03-5.13 (m, 6 H), 5.27 (br d, 1 H), 7.35 (m, 15 H), 7.95 (br d, 1 H) ; MS (FAB) m/z 576 (M+H), 598 (M+Na).

후처리

  1. customThe TFA is removed
  2. washwashed with saturated NaHCO3 solution
  3. customDrying
  4. customremoval of the solvent

출처 및 근거

ORD 기록
ord-23a760d0ac7f4736a865e18119dacb62
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05658945

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