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4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → (S)-N-(2'-amino-3-chloro-1-fluoro-5',6'-dihydrospiro[chromeno[2,3-c]pyridine-5,4'-[1,3]oxazin]-7-yl)-5-chloropicolinamide

HRID 931642
ノート
印刷プレビュー

反応式

HRID 931642 の反応式
[Cl:1][C:2]1[N:7]=[C:6]([F:8])[C:5]2[O:9][C:10]3[C:15]([C@@:16]4([CH2:21][CH2:20][O:19][C:18]([NH2:22])=[N:17]4)[C:4]=2[CH:3]=1)=[CH:14][C:13]([NH2:23])=[CH:12][CH:11]=3.[Cl:24][C:25]1[CH:26]=[CH:27][C:28]([C:31](O)=[O:32])=[N:29][CH:30]=1.[Cl-].COC1N=C(OC)N=C([N+]2(C)CCOCC2)N=1>>[NH2:22][C:18]1[O:19][CH2:20][CH2:21][C@:16]2([C:4]3[CH:3]=[C:2]([Cl:1])[N:7]=[C:6]([F:8])[C:5]=3[O:9][C:10]3[C:15]2=[CH:14][C:13]([NH:23][C:31](=[O:32])[C:28]2[CH:27]=[CH:26][C:25]([Cl:24])=[CH:30][N:29]=2)=[CH:12][CH:11]=3)[N:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 27340594-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 27628725-Chloro-2-picolinic acidHCID 90158687(S)-3-chloro-1-fluoro-5',6'-dihydrospiro[chromeno[2,3-c]pyridine-5,4'-[1,3]oxazine]-2',7-diamine

生成物 1

HCID 71542226(S)-N-(2'-amino-3-chloro-1-fluoro-5',6'-dihydrospiro[chromeno[2,3-c]pyridine-5,4'-[1,3]oxazin]-7-yl)-5-chloropicolinamide収率 37.9%

実験手順

A mixture of (S)-3-chloro-1-fluoro-5′,6′-dihydrospiro[chromeno[2,3-c]pyridine-5,4′-[1,3]oxazine]-2′,7-diamine (0.048 g, 0.143 mmol) and 5-chloro-2-pyridinecarboxylic acid (0.025 g, 0.158 mmol) was purged with N2 followed by the addition of THF (2 mL) and MeOH (0.5 mL). 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (0.046 g, 0.158 mmol) was added in one portion and the resulting reaction mixture was stirred at rt for 3 h. The reaction mixture was quenched with saturated NaHCO3, diluted with water and extracted with EtOAc. The combined organics were dried over Na2SO4, filtered, concentrated and chromatographed on silica gel using 0-4% MeOH/DCM and repurified by HPLC to afford (S)—N-(2′-amino-3-chloro-1-fluoro-5′,6′-dihydrospiro[chromeno[2,3-c]pyridine-5,4′-[1,3]oxazin]-7-yl)-5-chloropicolinamide as a white solid (0.0258 g, 0.054 mmol, 37.9% yield). MS m/z=474.0 [M+H]+.

後処理

  1. customwas purged with N2
  2. additionfollowed by the addition of THF (2 mL) and MeOH (0.5 mL)
  3. customthe resulting reaction mixture
  4. customThe reaction mixture was quenched with saturated NaHCO3
  5. additiondiluted with water
  6. extractionextracted with EtOAc
  7. dry with materialThe combined organics were dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customchromatographed on silica gel using 0-4% MeOH/DCM
  11. customrepurified by HPLC

出典と根拠

ORDレコード
ord-3ad92ba5725d46858b9c6f64a69deb74
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296759B2

反応ノート

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