M-Cresol → HCID 178495946, compound

HRID 616362Notes

Reaction equation

HRID 616362 reaction equation
[CH:1]1[C:6]([OH:7])=[CH:5][CH:4]=[CH:3][C:2]=1[CH3:8].[N:9]#[N:10].Cl.[CH3:12][O:13][C:14]1[CH:15]=[C:16]2[C:21](=[CH:22][C:23]=1[O:24][CH3:25])[CH:20]=[C:19]([S:26]([NH:29][C@H:30]([C:38]([N:40]([CH2:45][CH2:46][O:47][CH3:48])[CH2:41][C:42]([Cl:44])=[O:43])=[O:39])[CH2:31][CH2:32][CH2:33][NH:34][C:35](=[NH:37])[NH2:36])(=[O:28])=[O:27])[CH:18]=[CH:17]2>>[N:9]#[N:10].[ClH:44].[C:2]1([CH3:8])[CH:3]=[CH:4][CH:5]=[C:6]([O:7][C:42](=[O:43])[CH2:41][N:40]([C:38](=[O:39])[C@H:30]([CH2:31][CH2:32][CH2:33][NH:34][C:35](=[NH:36])[NH2:37])[NH:29][S:26]([C:19]2[CH:18]=[CH:17][C:16]3[C:21](=[CH:22][C:23]([O:24][CH3:25])=[C:14]([O:13][CH3:12])[CH:15]=3)[CH:20]=2)(=[O:28])=[O:27])[CH2:45][CH2:46][O:47][CH3:48])[CH:1]=1

Participants

3

Conditions

Temperature
90 °C

Procedure

A mixture of 2.00 g of m-cresol and N2 -(6, 7-dimethoxy-2-naphthylsulfonyl)-L-arginyl-N-(2-methoxyethyl)glycyl chloride hydrochloride obtained above was heated at 90° C for 50 minutes. At the end of this period, the reaction mixture was cooled, washed several times with dry ethyl ether, and then dissolved in 10 ml of dry ethyl alcohol. Addition of cold dry ethyl ether resulted in a precipitate which was washed several times with dry ethyl ether to give 2.12 g (86 percent) of N2 -(6, 7-dimethoxy-2-naphthylsulfonyl)-L-arginyl-N-(2-methoxyethyl)glycine m-tolyl ester hydrochloride in the form of a powder.

Workup

  1. customobtained
  2. temperatureAt the end of this period, the reaction mixture was cooled
  3. washwashed several times with dry ethyl ether
  4. dissolutiondissolved in 10 ml of dry ethyl alcohol
  5. additionAddition of cold dry ethyl ether
  6. customresulted in a precipitate which
  7. washwas washed several times with dry ethyl ether

Sources & evidence

ORD record
ord-b23b58e678334911801814feeb3244e0
Source dataset
uspto-grants-1978_02
Patent number
US04073892

Reaction notes

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