Caffeic Acid → HCID 18711615, 화합물

HRID 278850

반응식

HRID 278850 반응식
C(O[C:6]([NH:8][C@H:9]([C:18]([NH:20][CH2:21][C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[C:24]([OH:29])[CH:23]=1)=[O:19])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)=[O:7])(C)(C)C.C(O)(=O)/[CH:31]=[CH:32]/[C:33]1[CH:40]=[CH:39][C:37]([OH:38])=[C:35]([OH:36])[CH:34]=1>>[C:6]([NH:8][C@H:9]([C:18]([NH:20][CH2:21][C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[C:24]([OH:29])[CH:23]=1)=[O:19])[CH2:10][C:11]1[CH:12]=[CH:13][C:14]([OH:17])=[CH:15][CH:16]=1)(=[O:7])/[CH:31]=[CH:32]/[C:33]1[CH:40]=[CH:39][C:37]([OH:38])=[C:35]([OH:36])[CH:34]=1

참가 물질

3

반응물 2

HCID 689043Caffeic AcidHCID 18711627HCID 18711627, 화합물

생성물 1

HCID 18711615HCID 18711615, 화합물수율 51.2%

실험 절차

The title compound was prepared from N-(N-tert-butoxycarbonyl-L-tyrosyl)-3,4-dihydroxybenzylamine (example 56, step A) (1.4 g, 3.3 mmol) according to the indications of example 3, for 2 h. The crude intermediate was coupled with caffeic acid (978 mg, 5.4 mmol) according to the indications of example 4. The crude product was purified by flash chromatography using 40-80% AcOEt/CH2Cl2 containing 1% AcOH to yield the title product as yellow crystals (784 mg, 47%).

후처리

  1. customThe crude product was purified by flash chromatography

출처 및 근거

ORD 기록
ord-57506a0334f94bb791230b8a5230b180
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06362165B1

연결된 노트

불러오는 중…