반응 #11051

ord-834073e0ca044b46a874997ac8390157

반응 방정식

OCc1ccccc1
Benzyl alcohol
CC(C)(C)OC(=O)[C@@H]1CCc2ncc(C(=O)O)c(=O)n21
carboxylic acid
CC(C)(C)OC(=O)[C@@H]1CCc2ncc(C(=O)O)c(=O)n21
(S)-6-(tert-butoxycarbonyl)-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-3-carboxylic acid
CCN(CC)CC
triethylamine
[N-]=[N+]=NP(=O)(c1ccccc1)c1ccccc1
DPPA
CC(C)(C)OC(=O)[C@@H]1CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
benzyl carbamate
수율 73.0%
CC(C)(C)OC(=O)[C@@H]1CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
tert-butyl (S)-3-{[(benzyloxy)carbonyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylate
수율 73.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 2 h
  2. 2
    온도the mixture was heated
  3. 3
    온도at reflux for an additional 3 h
  4. 4
    농축The mixture was concentrated in vacuo
  5. 5
    기타the oil obtained
  6. 6
    기타was purified by flash chromatography (50 to 100% EtOAc/hexanes)

실험 절차

A solution of carboxylic acid 1f (11.4 g, 40.7 mmol), triethylamine (5.67 mL, 40.7 mmol), and DPPA (8.86 mL, 40.7 mmol) in 180 mL 1,4-dioxane was heated at reflux for 2 h. Benzyl alcohol (4.67 mL, 45 mmol) was added and the mixture was heated at reflux for an additional 3 h. The mixture was concentrated in vacuo and the oil obtained was purified by flash chromatography (50 to 100% EtOAc/hexanes) to provide 11.13 g (73%) of the benzyl carbamate (1 g) as a tan solid. 1H NMR (300 MHz, CDCl3) δ 8.67 (br s, 1H), 7.39–7.34 (m, 5H), 5.21 (s, 2H), 4.98 (dd, J=9.6, 3.0, 1H), 3.23–2.98 (m, 2H), 2.63–2.49 (m, 1H), 2.37–2.23 (m, 1H), 1.48 (s, 9H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094783B2uspto-grants-2006_08