Trifluoroacetic acid → HCID 178514772、化合物

HRID 1390710

反応式

HRID 1390710 の反応式
C1(=O)N(CS(Cl)(=O)=O)C(=O)C2=CC=CC=C12.C1(=O)N(CCS(Cl)(=O)=O)C(=O)C2=CC=CC=C12.C(NS(CN1C(=O)C2=CC=CC=C2C1=O)(=O)=O)(C)(C)C.C([NH:58][S:59]([CH2:62][N:63]1[C:67]([SH:68])=[N:66][N:65]=[N:64]1)(=[O:61])=[O:60])(C)(C)C.FC(F)(F)C(O)=O>>[S:59]([CH2:62][N:63]1[C:67]([SH:68])=[N:66][N:65]=[N:64]1)(=[O:61])(=[O:60])[NH2:58]

参加物

6

反応物 5

HCID 6422Trifluoroacetic acidHCID 3087392-Phthalimidoethanesulfonyl chlorideHCID 21315191(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)methanesulfonyl chlorideHCID 54174780N-t-butylphthalimidomethanesulfonamideHCID 178449998HCID 178449998、化合物2 回

生成物 1

HCID 178514772HCID 178514772、化合物

実験手順

When phthalimidomethanesulfonyl chloride is substituted in the procedure of Example 3 for 2-phthalimidoethanesulfonyl chloride, N-t-butylphthalimidomethanesulfonamide is prepared which is converted to 1-N-t-butylsulfamoylmethyltetrazole-5-thiol as described therein. Treatment of 1-N-t-butylsulfamoylmethyltetrazole-5-thiol with trifluoroacetic acid as described in Example 3 gives 1-sulfamoylmethyltetrazole-5-thiol.

後処理

  1. customis prepared which

出典と根拠

ORDレコード
ord-6a12ee21dcfd4585947ce72ceeb97512
出典データセット
uspto-grants-1979_02
特許番号
US04139701

関連ノート

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