Tributyltin azide → N-Ethyl-N'-[6-(2H-1,2,3,4-tetraazol-5-yl)-1,3-benzothiazol-2-yl]urea

HRID 9175

反応式

HRID 9175 の反応式
[C:1]([C:3]1[CH:17]=[CH:16][C:6]2[N:7]=[C:8]([NH:10][C:11]([NH:13][CH2:14][CH3:15])=[O:12])[S:9][C:5]=2[CH:4]=1)#[N:2].[N:18]([Sn](CCCC)(CCCC)CCCC)=[N+:19]=[N-:20]>O1CCCC1>[CH2:14]([NH:13][C:11]([NH:10][C:8]1[S:9][C:5]2[CH:4]=[C:3]([C:1]3[N:18]=[N:19][NH:20][N:2]=3)[CH:17]=[CH:16][C:6]=2[N:7]=1)=[O:12])[CH3:15]

参加物

4

反応物 2

HCID 4984872Tributyltin azideHCID 21985533N-(6-Cyano-1,3-benzothiazol-2-yl)-N'-ethylurea

生成物 1

HCID 21985643N-Ethyl-N'-[6-(2H-1,2,3,4-tetraazol-5-yl)-1,3-benzothiazol-2-yl]urea

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

About 30 mg N-(6-cyano-1,3-benzothiazol-2-yl)-N′-ethylurea was charged into about 5 mL dry tetrahydrofuran. Added about 2 g of azidotributylstannane then refluxed for about 48–72 hours. The solvent was removed under reduced pressure then the crude oil was taken up in dichloromethane. About 0.5 mL of dilute aqueous hydrochloric acid was added and a white precipitate formed. This was allowed to sit for about 30 minutes then the precipitate was collected by filtration, washed with warm THF then dried under vacuum. 1H NMR 1.10 (t, 3H), 3.2 (m, 2H), 6.76 (br s, 1H), 7.78 (d, 1H), 8.0 (d, 1H), 8.58 (s, 1H), 10.91 (s, 1H); LC/MS 1.37 min, 290 (M+1).

後処理

  1. temperaturethen refluxed for about 48–72 hours
  2. customThe solvent was removed under reduced pressure
  3. additionAbout 0.5 mL of dilute aqueous hydrochloric acid was added
  4. customa white precipitate formed
  5. filtrationthe precipitate was collected by filtration
  6. washwashed with warm THF
  7. customthen dried under vacuum
  8. customLC/MS 1.37 min, 290 (M+1)

出典と根拠

ORDレコード
ord-1c22368b0e704f58812f062c12896e4b
出典データセット
uspto-grants-2006_08
特許番号
US07091227B2

関連ノート

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