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Hydrochloric Acid → N-[4-(5-carboxypentylcarbamoyl)-cyclohexylmethyl]-2-(methylcarbamoyl)-ethylthiosuccinimide

HRID 260221
ノート
印刷プレビュー

反応式

HRID 260221 の反応式
[CH3:1][NH:2][C:3](=[O:9])[CH2:4][CH2:5][C:6](=[S:8])C.[OH-].[K+].Cl.[N+]([C:16]1[CH:24]=[CH:23][CH:22]=[CH:21][C:17]=1[C:18]([OH:20])=O)([S-])=S.C1C(SSC2C=CC([N+]([O-])=O)=C(C(O)=O)C=2)=CC(C(O)=O)=C([N+]([O-])=O)C=1.[CH2:51]1[CH:56]([CH2:57][N:58]2C(=O)C=CC2=O)CC[CH:53]([C:65]([O:67]N2C(=O)CCC2=O)=[O:66])[CH2:52]1.C([O-])(=O)CCCCC.[CH3:83][NH:84][C:85](=[O:89])[CH2:86][CH2:87]S>CO.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>[C:65]([CH2:53][CH2:52][CH2:51][CH2:56][CH2:57][NH:58][C:18]([CH:17]1[CH2:16][CH2:24][CH:23]([CH2:1][N:2]2[C:3](=[O:9])[CH2:4][CH:5]([CH2:87][CH2:86][C:85](=[O:89])[NH:84][CH3:83])[C:6]2=[S:8])[CH2:22][CH2:21]1)=[O:20])([OH:67])=[O:66]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 7

HCID 313Hydrochloric AcidHCID 62545,5'-Dithiobis(2-nitrobenzoic Acid)HCID 14797Potassium HydroxideHCID 6429063-Mercapto-N-methylpropanamideHCID 21865436(2-Carboxyphenyl)-sulfanylidene-sulfidoazaniumHCID 54417257N-methyl-(3-thioacetyl)propionamide
HCID 131719433
SMCC caproate

生成物 1

HCID 88051188N-[4-(5-carboxypentylcarbamoyl)-cyclohexylmethyl]-2-(methylcarbamoyl)-ethylthiosuccinimide

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 62657Potassium Phosphate, Tribasic溶媒2 回

実験手順

The thiol ester of N-methyl-(3-thioacetyl)-propionamide (4.6 mg, 3.1×10-5 mol, see Example 3) was hydrolyzed by the addition of 0.62 ml of 0.12M KOH in 80% methanol. After 10 min, 0.3 ml of 0.5M potassium phosphate, pH 7 was added to the thiol compound and the pH adjusted to 7.5 with 1N hydrochloric acid. The thiol concentration was 34 mM (determined by reaction with dithionitrobenzoic acid, DTNB). SMCC-caproate (8.7 mg, 2.5×10-5 mol) was dissolved in 0.4 ml of 0.5M potassium phosphate, pH 7.0, and the N-methyl-(3-mercapto)propionamide solution (0.742 ml, 2.5×10-5 mol) added. The solution was gassed with argon and the tube sealed. After 12 hr at room temperature, no thiol remained and the solvent was removed in vacuo. The residue was dissolved in 0.117 ml water to make a 213 mM solution of the desired compound (see FIG. 1D).

後処理

  1. customthe tube sealed
  2. waitAfter 12 hr at room temperature
  3. customthe solvent was removed in vacuo
  4. dissolutionThe residue was dissolved in 0.117 ml water

出典と根拠

ORDレコード
ord-84a161067fa441ecbd903aa4c6b6a1a5
出典データセット
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05525524

反応ノート

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