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Triacetoxyperiodinane → HCID 86634725, 화합물

HRID 910959
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HRID 910959 반응식
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[CH3:23][C:24]1[N:25]=[C:26]([NH:29][C:30]2[N:35]=[CH:34][C:33]([CH2:36][OH:37])=[C:32]([O:38][C:39]3[C:48]4[C:43](=[CH:44][CH:45]=[CH:46][CH:47]=4)[CH:42]=[CH:41][CH:40]=3)[CH:31]=2)[S:27][CH:28]=1>C1COCC1.CCOCC.[OH-].[Na+]>[CH3:23][C:24]1[N:25]=[C:26]([NH:29][C:30]2[CH:31]=[C:32]([O:38][C:39]3[C:48]4[C:43](=[CH:44][CH:45]=[CH:46][CH:47]=4)[CH:42]=[CH:41][CH:40]=3)[C:33]([CH:36]=[O:37])=[CH:34][N:35]=2)[S:27][CH:28]=1
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참가 물질

6

반응물 2

HCID 159087TriacetoxyperiodinaneHCID 24826338HCID 24826338, 화합물

생성물 1

HCID 86634725HCID 86634725, 화합물수율 93.5%

시약·촉매·용매 3

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매HCID 14798Sodium Hydroxide용매

실험 절차

To a solution of Dess Martin periodane (1.30 g, 3.05 mmol) in THF (5 mL) at 0° C. was added a solution of (6-(4-methylthiazol-2-ylamino)-4-(naphthalen-1-yloxy)pyridin-3-yl)methanol (0.925 g, 2.55 mmol). The mixture was warmed to room temperature and stirred for 30 minutes, diluted with ether and hydrolyzed with 1N NaOH (40 mL). The mixture was extracted with ether, washed with brine, dried, and concentrated to afford 6-(4-methylthiazol-2-ylamino)-4-(naphthalen-1-yloxy)nicotinaldehyde (0.860 g, 93.5% yield) as a light yellow solid. 1H NMR (DMSO d6) δ 11.28 (bs, 1H), 10.40 (s, 1H), 8.75 (s, 1H), 8.09 (d, 1H), 7.98 (d, 1H), 7.92 (d, 1H), 7.55-7.68 (m, 3H), 7.49 (d, 1H), 6.62 (s, 1H), 6.26 (bs, 1H), 2.13 (s, 3H).

후처리

  1. extractionThe mixture was extracted with ether
  2. washwashed with brine
  3. customdried
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-394b506e41064e3cb08197f4f7776539
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022222B2

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