ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

4-Methylmorpholine → Methyl-4-{5-[2-(2-anilino-1,3-benzoxazol6-yl)-acetylamino]-2-methoxyphenoxy}-3-methyl-butanoate

HRID 2305622
ノート
印刷プレビュー

反応式

HRID 2305622 の反応式
[C:1]1([NH:7][C:8]2[O:9][C:10]3[CH:16]=[C:15]([CH2:17][C:18]([OH:20])=O)[CH:14]=[CH:13][C:11]=3[N:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:21][CH:22]([CH:27]([O:29][C:30]1[CH:35]=[C:34]([NH2:36])[CH:33]=[CH:32][C:31]=1[O:37][CH3:38])C)[C:23](OC)=O.[OH:39][C:40]1C2N=NNC=2C=CC=1.CN1CC[O:53][CH2:52]C1.Cl.CN(C)CCCN=C=NCC>CN(C)C=O.O>[CH3:52][O:53][C:40](=[O:39])[CH2:23][CH:22]([CH3:21])[CH2:27][O:29][C:30]1[CH:35]=[C:34]([NH:36][C:18](=[O:20])[CH2:17][C:15]2[CH:14]=[CH:13][C:11]3[N:12]=[C:8]([NH:7][C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)[O:9][C:10]=3[CH:16]=2)[CH:33]=[CH:32][C:31]=1[O:37][CH3:38]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 79724-MethylmorpholineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 111498372-Phenylaminobenzoxazol-6-acetic acidHCID 53892958Methyl 2-methyl-3-(2-methoxy-5-aminophenoxy)butyrateHCID 178418300HCID 178418300、化合物

生成物 1

HCID 54563344
Methyl-4-{5-[2-(2-anilino-1,3-benzoxazol6-yl)-acetylamino]-2-methoxyphenoxy}-3-methyl-butanoate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

To a mixture of 2-phenylaminobenzoxazole-6-acetic acid(0.067 g), methyl 2-methyl-3-(2-methoxy-5-aminophenoxy)butyrate(0.057 g), hydroxybenzotriazole (0.067 g), and N-methylmorpholine(0.05 ml) in dimethylformamide(0.25 ml) was added 1-(3-dimethylaminopropyl)3-ethylcarbodiimide hydrochloride(0.095 g). The resultant mixture was stirred for 48 hrs then added to water and extracted with ethyl acetate. The organic layer was separated, washed with aqueous acetic acid, brine, aqueous sodium bicarbonate (2 times), dried and evaporated to dryness. The residue was purified by purified by chromatography on silica using an increasingly polar mixture of ethyl acetateldichloromethane and the appropriate fraction yielded, after evaporation to dryness, a solid which was triturated with a mixture of diethylether/hexane to give the product (0.08 g) as a purple-pink solid.

後処理

  1. extractionextracted with ethyl acetate
  2. customThe organic layer was separated
  3. washwashed with aqueous acetic acid, brine, aqueous sodium bicarbonate (2 times)
  4. customdried
  5. customevaporated to dryness
  6. customThe residue was purified
  7. customby purified by chromatography on silica using
  8. additionan increasingly polar mixture of ethyl acetateldichloromethane
  9. customthe appropriate fraction yielded
  10. customafter evaporation to dryness
  11. customa solid which was triturated with a mixture of diethylether/hexane

出典と根拠

ORDレコード
ord-40cbb133dd7a46b0b2b9a6dc9d61c7f1
出典データセット
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06441012B1

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート