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Ammonia → (RS)-5-Chloro-pyridine-2-carboxylic acid [3-(5-amino-3-cyclopropyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-amide

HRID 1929505
ノート
印刷プレビュー

反応式

HRID 1929505 の反応式
[NH3:1].[CH:2]1([C:5]2([C:12]3[CH:13]=[C:14]([NH:19][C:20]([C:22]4[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][N:23]=4)=[O:21])[CH:15]=[CH:16][C:17]=3[F:18])[CH2:10][O:9][CH2:8][C:7](=S)[NH:6]2)[CH2:4][CH2:3]1.C(OO)CCC>CO>[NH2:1][C:7]1[CH2:8][O:9][CH2:10][C:5]([C:12]2[CH:13]=[C:14]([NH:19][C:20]([C:22]3[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][N:23]=3)=[O:21])[CH:15]=[CH:16][C:17]=2[F:18])([CH:2]2[CH2:4][CH2:3]2)[N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 222AmmoniaHCID 123219n-ButylhydroperoxideHCID 86651226(RS)-5-chloro-pyridine-2-carboxylic acid [3-(3-cyclopropyl-5-thioxo-morpholin-3-yl)-4-fluoro-phenyl]-amide

生成物 1

HCID 50992036(RS)-5-Chloro-pyridine-2-carboxylic acid [3-(5-amino-3-cyclopropyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-amide

試薬・触媒・溶媒 1

HCID 887Methanol
溶媒
2 回

実験手順

A solution of ammonia in methanol (7 M) (5.1 ml, 35 mmol) was added to a suspension of (RS)-5-chloro-pyridine-2-carboxylic acid [3-(3-cyclopropyl-5-thioxo-morpholin-3-yl)-4-fluoro-phenyl]-amide (=5-chloro-pyridine-2-carboxylic acid [3-((RS)-3-cyclopropyl-5-thioxo-morpholin-3-yl)-4-fluoro-phenyl]-amide) (0.240 g, 0.59 mmol) in methanol (18 ml). Thereafter, tent-butyl hydroperoxide (70% in water) (0.81 ml, 5.9 mmol) was added at room temperature and the mixture stirred for 16 hours. For the workup, the clear solution was evaporated at reduced pressure. The residue was purified by chromatography on silica gel using a 80:10:1-mixture of ethyl acetate, methanol, and ammoniumhydroxide as the eluent. The pure fractions were combined and evaporated, then the residue was treated with a mixture of dichloromethane and water. After evaporation of the organic layer, the 5-chloro-pyridine-2-carboxylic acid [3-((RS)-5-amino-3-cyclopropyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-amide (22) was obtained as a white solid (99 mg, 43% of theory). Mass (calculated) C19H18ClFN4O2S [388.828]; (found) [M+H]+=389.

後処理

  1. customFor the workup, the clear solution was evaporated at reduced pressure
  2. customThe residue was purified by chromatography on silica gel using a 80:10
  3. customevaporated
  4. additionthe residue was treated with a mixture of dichloromethane and water
  5. customAfter evaporation of the organic layer

出典と根拠

ORDレコード
ord-a054351e9761491984246872f4d0997a
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08188079B2

反応ノート

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