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1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 2-(3-hydroxypyrrolidin-1-yl)-1,3-thiazole-5-carboxylate

HRID 2355057
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HRID 2355057 반응식
Br[C:2]1[S:3][C:4]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][N:6]=1.[NH:11]1[CH2:15][CH2:14][CH:13]([OH:16])[CH2:12]1.C1CCN2C(=NCCC2)CC1>O1CCOCC1.O>[OH:16][CH:13]1[CH2:14][CH2:15][N:11]([C:2]2[S:3][C:4]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][N:6]=2)[CH2:12]1
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참가 물질

6

반응물 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 982104-HydroxypyrrolidineHCID 2773502Methyl 2-bromothiazole-5-carboxylate

생성물 1

HCID 68452743Methyl 2-(3-hydroxypyrrolidin-1-yl)-1,3-thiazole-5-carboxylate

시약·촉매·용매 2

HCID 962Water용매HCID 312751,4-Dioxane용매

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온도
82.5 °C

실험 절차

A mixture of methyl 2-bromo-1,3-thiazole-5-carboxylate (3 g, 13.5 mmol), 3-pyrrolidinol (1.3 g, 14.9 mmol) and DBU (4.1 mL, 27 mmol) in dioxane (50 mL) was heated at 80-85° C. overnight. After cooling, the mixture was diluted with water and extracted five times with EtOAc. The combined EtOAc extracts were washed with water, dried (Na2SO4) and concentrated to give the crude title compound as a light brown solid. 1H NMR (400 MHz, acetone-d6): δ 7.83 (s, 1H), 4.65 (m, 1 H), 4.33 (m, 1 H), 3.79 (s, 3 H), 3.67-3.45 (m, 4 H), 2.29-2.19 (m, 1 H), 2.11 (m, 1 H).

후처리

  1. temperatureAfter cooling
  2. extractionextracted five times with EtOAc
  3. washThe combined EtOAc extracts were washed with water
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0ee2fea293eb49d7b3ceb6271daa3fbc
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754745B2

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