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Propylphosphonic anhydride → (2R)-2-amino-2-methyl-N-[6-[(2,4,4-trimethyl-3,1-benzoxazin-5-yl)oxy]-3-pyridyl]butanamide

HRID 527663
ノート
印刷プレビュー

反応式

HRID 527663 の反応式
[CH3:1][C:2]1[O:7][C:6]([CH3:9])([CH3:8])[C:5]2[C:10]([O:14][C:15]3[N:20]=[CH:19][C:18]([NH2:21])=[CH:17][CH:16]=3)=[CH:11][CH:12]=[CH:13][C:4]=2[N:3]=1.Cl.[NH2:23][C@:24]([CH3:30])([CH2:28][CH3:29])[C:25](O)=[O:26].C(P1(=O)OP(CCC)(=O)OP(CCC)(=O)O1)CC>C(OCC)(=O)C.CC#N.C(OCC)(=O)C.O>[NH2:23][C@:24]([CH3:30])([CH2:28][CH3:29])[C:25]([NH:21][C:18]1[CH:19]=[N:20][C:15]([O:14][C:10]2[C:5]3[C:6]([CH3:8])([CH3:9])[O:7][C:2]([CH3:1])=[N:3][C:4]=3[CH:13]=[CH:12][CH:11]=2)=[CH:16][CH:17]=1)=[O:26]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 111923Propylphosphonic anhydrideHCID 17998883(R)-2-Amino-2-methylbutanoic acid hydrochlorideHCID 679602016-[(2,4,4-Trimethyl-3,1-benzoxazin-5-yl)oxy]pyridin-3-amine2 回

生成物 1

HCID 67959970(2R)-2-amino-2-methyl-N-[6-[(2,4,4-trimethyl-3,1-benzoxazin-5-yl)oxy]-3-pyridyl]butanamide収率 57.5%

試薬・触媒・溶媒 3

HCID 962
Water
溶媒
HCID 8857Ethyl Acetate溶媒2 回
HCID 21930812Acetonitrile ethyl acetate溶媒

反応条件

温度
80 °C

実験手順

To a suspension of 6-[(2,4,4-trimethyl-3,1-benzoxazin-5-yl)oxy]pyridin-3-amine (Intermediate 204, 185 mg, 0.65 mmol) and (R)-2-amino-2-methyl-butanoic acid hydrochloride (100 mg, 0.67 mmol) in ethyl acetate/MeCN (2 mL, 1:3 v/v mixture), a 50% w/w solution in ethyl acetate of T3P (0.43 mL) was added drop wise at 0° C. The mixture was then heated at 60° C. for 3 hours and at 80° C. for 4.5 hours. The mixture was cooled to room temperature diluted with water (5 mL) and ethyl acetate (10 mL), Two phases were separated and the aqueous one was treated with a saturated solution of NaHCO3 (pH=8) and back-extracted with ethyl acetate (2×10 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated and the residue was purified by flash chromatography on silica gel using cyclohexane/ethyl acetate 20:80 as eluent affording the title compound (143 mg) as a yellow foam.

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. customwere separated
  3. additionthe aqueous one was treated with a saturated solution of NaHCO3 (pH=8)
  4. extractionback-extracted with ethyl acetate (2×10 mL)
  5. dry with materialThe combined organic layers were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe residue was purified by flash chromatography on silica gel

出典と根拠

ORDレコード
ord-e35ce4eb4320490882673310fd91ddb7
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346790B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート