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4-Nitrobenzoic Acid → (S)-7-benzyl-1-(5-(4-nitrobenzoyloxy)hexyl)-3-methylxanthine

HRID 1814975
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HRID 1814975 반응식
N(C(OCC)=O)=NC(OCC)=O.[CH2:13]([N:20]1[C:28]2[C:27](=[O:29])[N:26]([CH2:30][CH2:31][CH2:32][CH2:33][C@H:34]([OH:36])[CH3:35])[C:25](=[O:37])[N:24]([CH3:38])[C:23]=2[N:22]=[CH:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[N+:39]([C:42]1[CH:50]=[CH:49][C:45]([C:46](O)=[O:47])=[CH:44][CH:43]=1)([O-:41])=[O:40].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[CH2:13]([N:20]1[C:28]2[C:27](=[O:29])[N:26]([CH2:30][CH2:31][CH2:32][CH2:33][C@@H:34]([O:36][C:46](=[O:47])[C:45]3[CH:44]=[CH:43][C:42]([N+:39]([O-:41])=[O:40])=[CH:50][CH:49]=3)[CH3:35])[C:25](=[O:37])[N:24]([CH3:38])[C:23]=2[N:22]=[CH:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 61084-Nitrobenzoic AcidHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 9885048(R)-7-benzyl-1-(5-hydroxyhexyl)-3-methylxanthine

생성물 1

HCID 53988311(S)-7-benzyl-1-(5-(4-nitrobenzoyloxy)hexyl)-3-methylxanthine수율 88.3%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

Diethyl azodicarboxylate (14.63 g, 84 mmol) was added dropwise to a solution of (R)-7-benzyl-1-(5-hydroxyhexyl)-3-methylxanthine (as prepared in Example 29) (20 g, 56 mmol), 4-nitrobenzoic acid (14 g, 84 mmol) and triphenylphosphine (22 g, 84 mmol) in tetrahydrofuran (200 ml). After stirring for 30 minutes, the reaction mixture was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with 30% ethyl acetate-hexane to provide (S)-7-benzyl-1-(5-(4-nitrobenzoyloxy)hexyl)-3-methylxanthine (25 g).

후처리

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. customThe residue was purified by flash chromatography on silica gel eluting with 30% ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-6a8ceb16a3044754822310254f86a316
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06878715B1

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