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Hydrochloric Acid → HCID 9948781、化合物

HRID 1245644
ノート
印刷プレビュー

反応式

HRID 1245644 の反応式
[H-].[Na+].Br[CH2:4][CH2:5][C:6]1[N:7]=[C:8]([NH:11][S:12]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[C:16]=2[CH3:22])(=[O:14])=[O:13])[S:9][CH:10]=1.OC1C=NC=CC=1.Cl>O1CCCC1>[Cl:21][C:17]1[C:16]([CH3:22])=[C:15]([S:12]([NH:11][C:8]2[S:9][CH:10]=[C:6]([CH:5]=[CH2:4])[N:7]=2)(=[O:14])=[O:13])[CH:20]=[CH:19][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 79713-HydroxypyridineHCID 24758Sodium hydrideHCID 11292384HCID 11292384、化合物

生成物 1

HCID 9948781HCID 9948781、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Sodium hydride (95% dry, 32 mg, 1.27 mmol) was added to a stirred solution of the product from Step 3 (240 mg, 0.61 mmol) and 3-hydroxypyridine (63 mg, 0.67 mmol) in tetrahydrofuran (10 mL) at 0° C. After 2 h at reflux temperature the reaction was neutralized by adding 2 M HCl and the product mixture was extracted with dichloromethane. The organic phase was dried (Na2SO4) and the solvent was evaporated. The crude material was purified by flash chromatography on silica gel gradient eluting with 2-5% acetone in dichloromethane giving the title compound as a solid (33 mg, 17%). MS (Ionspray, [M+H]+) m/z 314; Anal. Calcd. (found) for C12H11ClN2O2S2: C 45.8 (45.0) % H 3.5 (3.9) %N 8.9(9.1) %.

後処理

  1. temperatureAfter 2 h at reflux temperature the reaction
  2. extractionthe product mixture was extracted with dichloromethane
  3. dry with materialThe organic phase was dried (Na2SO4)
  4. customthe solvent was evaporated
  5. customThe crude material was purified by flash chromatography on silica gel gradient
  6. washeluting with 2-5% acetone in dichloromethane giving the title compound as a solid (33 mg, 17%)

出典と根拠

ORDレコード
ord-2fb957e7f69847468ab7c81ad73de12a
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07125900B2

反応ノート

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