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Acetic Acid → HCID 178514862、化合物

HRID 605003
ノート
印刷プレビュー

反応式

HRID 605003 の反応式
Cl.Cl.[NH:3]1[CH2:8][CH2:7][CH:6]([C:9]2[N:13]=[C:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=3)[NH:11][N:10]=2)[CH2:5][CH2:4]1.[CH3:20][N:21]1[CH:30]=[CH:29][C:28]2[N:27]=[C:26]([C:31]3[CH:38]=[CH:37][C:34](C=O)=[CH:33][CH:32]=3)[C:25]([C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)=[CH:24][C:23]=2[C:22]1=[O:45].C(N(CC)CC)C.[C:53](O)(=[O:55])C.[C:57](O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>CN(C=O)C>[OH:55][CH2:53][CH2:20][N:21]1[CH:30]=[CH:29][C:28]2[N:27]=[C:26]([C:31]3[CH:38]=[CH:37][C:34]([CH2:57][N:3]4[CH2:8][CH2:7][CH:6]([C:9]5[N:13]=[C:12]([C:14]6[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=6)[NH:11][N:10]=5)[CH2:5][CH2:4]4)=[CH:33][CH:32]=3)[C:25]([C:39]3[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=3)=[CH:24][C:23]=2[C:22]1=[O:45]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 176Acetic AcidHCID 8471TriethylamineHCID 5049666Sodium triacetoxyborohydride2 回HCID 866249424-(6-Methyl-5-oxo-3-phenyl-5,6-dihydro-1,6-naphthyridin-2-yl)benzaldehydeHCID 1784785342-(5-Piperidin-4-yl-4h-1,2,4-triazol-3-yl)-pyridine dihydrochloride

生成物 1

HCID 178514862
HCID 178514862、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 2-(3-piperidin-4-yl-1H-1,2,4-triazol-5-yl)pyridine dihydro-chloride (21 mg, 0.07 mmol) and 4-(6-methyl-5-oxo-3-phenyl-5,6-dihydro-1,6-naphthyridin-2-yl)benzaldehyde (17 mg, 0.046 mmol) in dry DMF (1.0 mL) was added triethyl-amine (25 mL, 0.18 mmol). After stirring for 10 minutes acetic acid (30 μL, 0.53 mmol) was added and the mixture was stirred at room temperature over night. Then sodium triacetoxy borohydride (17 mg, 0.08 mmol) was added in one portion. After monitoring by LC/MS it was determined the reaction was not complete and additional sodium triacetoxy borohydride (5 mg, 0.02 mmol)) were added and the reaction was stirred over night. This reaction mixture was concentrated to a smaller volume and adsorbed on silica gel and purified by column chromatography eluting with 20-100% ethyl acetate and then 0.5-9% methanol/ethyl acetate (sat'd NH3). The appropriate fractions were combined and the solvents removed in vacuo. The residue was triturated with diethyl ether to give pure title compound as a pale yellow solid. 1H NMR (500 MHz, CDCl3): δ 8.69 (1H, s), 8.64 (1H, d, J=4.4 Hz), 8.14 (1H, d, J=7.5 Hz), 7.83 (1H, t, J=7.5 Hz), 7.35-7.41 (5H, m), 7.21-7.28 (6H, m), 6.89 (1H, d, J=7.6 Hz), 4.24 (2H, t, J=4.8 Hz), 4.04 (2H, t, J=4.6 Hz), 3.58 (2H, vbr s), 3.00 (2H, vbr s), 2.86 (1H, m), 2.02-2.17 (4H, m). m/e (m+1): 584.1, 292.7 [(m+2)/2].

後処理

  1. additionwas added
  2. stirringthe reaction was stirred over night
  3. concentrationThis reaction mixture was concentrated to a smaller volume
  4. custompurified by column chromatography
  5. washeluting with 20-100% ethyl acetate
  6. customthe solvents removed in vacuo
  7. customThe residue was triturated with diethyl ether

出典と根拠

ORDレコード
ord-743f26b9c78743699ffafaa9d9b7951d
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07910561B2

反応ノート

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