Oxalic Acid → (+/-)-1-[3-[[(3,4-Dihydro-2h-1-benzopyran-2-yl)-methyl]amino]propyl]tetrahydro-2(1h)-pyrimidinethione ethanedioate

HRID 2298798노트

반응식

HRID 2298798 반응식
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH2:4][CH2:3][CH:2]1[CH:11]=O.[NH2:13][CH2:14][CH2:15][CH2:16][N:17]1[CH2:22][CH2:21][CH2:20][NH:19][C:18]1=[S:23].[C:24]([OH:29])(=[O:28])[C:25]([OH:27])=[O:26]>CO.[Pd]>[C:24]([OH:29])(=[O:28])[C:25]([OH:27])=[O:26].[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH2:4][CH2:3][CH:2]1[CH2:11][NH:13][CH2:14][CH2:15][CH2:16][N:17]1[CH2:22][CH2:21][CH2:20][NH:19][C:18]1=[S:23]

참가 물질

6

반응물 3

HCID 971Oxalic Acid2회HCID 20627851HCID 20627851, 화합물HCID 225732481-(3-aminopropyl)tetrahydro-2(1H)-pyrimidinethione

생성물 1

HCID 22573245(+/-)-1-[3-[[(3,4-Dihydro-2h-1-benzopyran-2-yl)-methyl]amino]propyl]tetrahydro-2(1h)-pyrimidinethione ethanedioate수율 7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of 3.4-dihydro-2H-1-benzopyran-2-carboxaldehyde (0.015 mol) and 1-(3-aminopropyl)tetrahydro-2(1H)-pyrimidinethione (0.01 mol) in methanol (150 ml) was hydrogenated for 2 days at room temperature (atmospheric pressure) with palladium on activated carbon (2 g) as a catalyst. After uptake of H2 (1 eq.), the catalyst was filtered off and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: C2Cl2/(CH3OH/NH3) 95/5). The pure fractions were collected and the solvent was evaporated. The residue (0.3 g) was dissolved in ethanol (30 ml) and converted into the ethanedioic acid salt (1:1 ) with ethanedioic acid (0.3 g; 0.0124 mol). The precipitate was filtered off and dried (vacuum), yielding 0.3 g (7%) of (±)-1-[3-[[(3,4-dihydro-2H-1-benzopyran-2-yl)-methyl]amino]propyl]tetrahydro-2(1H)-pyrimidinethione ethanedioate(1:1); mp. 217.6° C. (comp. 14).

후처리

  1. filtrationAfter uptake of H2 (1 eq.), the catalyst was filtered off
  2. customthe filtrate was evaporated
  3. customThe residue was purified by column chromatography over silica gel (eluent: C2Cl2/(CH3OH/NH3) 95/5)
  4. customThe pure fractions were collected
  5. customthe solvent was evaporated
  6. dissolutionThe residue (0.3 g) was dissolved in ethanol (30 ml)
  7. filtrationThe precipitate was filtered off
  8. customdried (vacuum)

출처 및 근거

ORD 기록
ord-2dcaf85f98d2454196f4db61e46f7a6d
출처 데이터셋
uspto-grants-2002_12
특허 번호
US06495547B1

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