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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-Phenylglycine ethyl ester → (4aR-cis)-1,2,3,4a,5,10b-Hexahydro-5,5-dimethyl-3-oxo-1-phenyl[1]benzopyrano[3,4-b][1,4]oxazine-9-carbonitrile

HRID 356676
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HRID 356676 반응식
C(OC(=O)CNC1C=CC=CC=1)C.C[Al](C)C.CC1(C)[C@@H]2O[C@@H]2C2C=C(C#N)C=CC=2O1.[C:33]([C:35]1[CH:36]=[CH:37][C:38]2[O:43][C:42]([CH3:45])([CH3:44])[C@H:41](O)[C@@H:40]([N:47]([CH2:54][C:55]([O:57]CC)=[O:56])[C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)[C:39]=2[CH:60]=1)#[N:34]>ClCCCl.C(OCC)(=O)C.C(Cl)(Cl)Cl.CO>[CH3:44][C:42]1([CH3:45])[C@@H:41]2[O:56][C:55](=[O:57])[CH2:54][N:47]([C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)[C@@H:40]2[C:39]2[CH:60]=[C:35]([C:33]#[N:34])[CH:36]=[CH:37][C:38]=2[O:43]1
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참가 물질

9

반응물 4

HCID 75190N-Phenylglycine ethyl esterHCID 10738551(3R-trans)-[(6-cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-yl)phenylamino]acetic acid, ethyl esterHCID 10987295(1aR,7bR)-2,2-Dimethyl-1a,7b-dihydro-2H-oxireno[2,3-c]chromene-6-carbonitrileHCID 16682925Trimethylaluminum

생성물 1

HCID 67799274
(4aR-cis)-1,2,3,4a,5,10b-Hexahydro-5,5-dimethyl-3-oxo-1-phenyl[1]benzopyrano[3,4-b][1,4]oxazine-9-carbonitrile

시약·촉매·용매 4

HCID 111,2-Dichloroethane용매HCID 887Methanol용매HCID 6212Chloroform용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of N-phenylglycine ethyl ester (900 mg, 5.0 mmol) in 1,2-dichloroethane (10 mL) under argon at 20° C. was treated with trimethylaluminum (3.0 mL, 2.0M in toluene, 6.0 mmol) over 1-2 minutes. After 15 minutes, (1aR-cis)-1a,7b-dihydro-2,2-dimethyl-2H-oxireno[c][1]benzopyran-6-carbonitrile (1.0 g, 5.0 mmol, title A compound of example 3) was added at once and stirring was continued for 1.5 hours. The mixture was diluted with ethyl acetate, quenched with a few drops of water and filtered through celite to remove gelatinous aluminum salts. The filtrate was washed with 5% sodium bicarbonate, water and brine, dried over anhydrous magnesium sulfate and concentrated. The residue was triturated with warm methanol to give warm methanol to give the title product (392 mg), mp 241°-243° C. [α]D =-129.1 ° (c=0.35 CHCl3). Analysis calculated for. C20H18N2O3 ·0.14 H2O: C,71.29; H,5.47; N, 8.31. Found: C, 71.05; H, 5.30; N, 8.55.

후처리

  1. waitwas continued for 1.5 hours
  2. customquenched with a few drops of water
  3. filtrationfiltered through celite
  4. customto remove gelatinous aluminum salts
  5. washThe filtrate was washed with 5% sodium bicarbonate, water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated
  8. customThe residue was triturated with warm methanol
  9. customto give

출처 및 근거

ORD 기록
ord-a24d7fadbac848f990d1434e8d45cd9f
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05837702

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