Thioglycerol → 2-(2,3-Dihydroxypropyldisulfanyl)-N-(4-sulfamoylphenyl) benzamide

HRID 3744

반응식

HRID 3744 반응식
[O:1]=[C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[S:4][N:3]1[C:11]1[CH:16]=[CH:15][C:14]([S:17]([NH2:20])(=[O:19])=[O:18])=[CH:13][CH:12]=1.O1CCCC1.[OH:26][CH:27]([CH2:30][OH:31])[CH2:28][SH:29]>CO>[OH:26][CH:27]([CH2:30][OH:31])[CH2:28][S:29][S:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:2]([NH:3][C:11]1[CH:16]=[CH:15][C:14]([S:17](=[O:19])(=[O:18])[NH2:20])=[CH:13][CH:12]=1)=[O:1]

참가 물질

5

반응물 3

HCID 7291ThioglycerolHCID 8028TetrahydrofuranHCID 4629384-(3-Oxo-1,2-benzothiazol-2-yl)benzenesulfonamide

생성물 1

HCID 108356092-(2,3-Dihydroxypropyldisulfanyl)-N-(4-sulfamoylphenyl) benzamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

This compound was prepared according to the method of Example 132 using a suspension of 0.46 g (1.5 mmol) of 4-(3-oxo-3H-benzo[d]isothiazol-2-yl) benzenesulfonamide in a mixture of 15 mL of methanol, and 15 mL of tetrahydrofuran and 2,3-dihydroxy-1-propanethiol. The product was washed with ether and dried in vacuo to give 0.61 g of the title compound, mp>260° C.

후처리

  1. customThis compound was prepared
  2. washThe product was washed with ether
  3. customdried in vacuo

출처 및 근거

ORD 기록
ord-039c45d2d6ad447186631f36b49d7ebe
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05734081

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