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4-Methylmorpholine → HCID 68643966, 화합물

HRID 2388694
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HRID 2388694 반응식
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CN1CCOCC1.CN([P+](ON1N=NC2C=CC=CC1=2)(N(C)C)N(C)C)C.F[P-](F)(F)(F)(F)F.[C:41]([O:45][C:46]([N:48]1[CH2:53][CH2:52][C:51]2[O:54][N:55]=[C:56]([C:57](O)=[O:58])[C:50]=2[CH2:49]1)=[O:47])([CH3:44])([CH3:43])[CH3:42]>CN(C)C=O>[N:1]1([C:57]([C:56]2[C:50]3[CH2:49][N:48]([C:46]([O:45][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:47])[CH2:53][CH2:52][C:51]=3[O:54][N:55]=2)=[O:58])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 79724-MethylmorpholineHCID 8082PiperidineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 576186225-(1,1-Dimethylethyl) 6,7-dihydroisoxazolo[4,5-c]pyridine-3,5(4H)-dicarboxylate

생성물 1

HCID 68643966HCID 68643966, 화합물

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

Piperidine (1.1 ml, 11.18 mmol), N-methylmorpholine (3.68 ml, 33.54 mmol) and BOP reagent (6.42 g, 14.53 mmol) were added to a solution of 5-(tert-butoxycarbonyl)-4,5,6,7-tetrahydroisoxazolo[4,5-c]pyridine-3-carboxylic acid (3 g, 11.18 mmol) in dry dimethylformamide (100 ml) and the reaction mixture was stirred at room temperature for 16 hours. The solution was then concentrated in vacuo, the residue was taken up in ethyl acetate and the mixture was washed with NaHCO3 solution and NaCl solution. The combined organic phases were dried with Na2SO4, filtered and concentrated in vacuo. Purification was carried out by chromatography on silica gel (100-200 mesh silica gel, 30% ethyl acetate in hexane). The yield was (71%).

후처리

  1. concentrationThe solution was then concentrated in vacuo
  2. washthe mixture was washed with NaHCO3 solution and NaCl solution
  3. dry with materialThe combined organic phases were dried with Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customPurification

출처 및 근거

ORD 기록
ord-5fa2baff715a4f97a340fc10e99c5e43
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268814B2

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