3-Mercaptopropionic Acid → HCID 23303066, compound

HRID 2289616Notes

Reaction equation

HRID 2289616 reaction equation
[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][N:6]=[C:5]([C:10](=[O:23])[C:11]2[N:18]3[C:14](=[N:15][C:16]4[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=43)[S:13][N:12]=2)[C:4]=1[CH3:24].S[CH2:26]CC(O)=O.[C:31](=[O:34])(O)[O-:32].[Na+]>CO.Cl>[NH:12]=[C:11]([N:18]1[C:17]2[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=2[N:15]=[C:14]1[SH:13])[C:10]([C:5]1[C:4]([CH3:24])=[C:3]([O:2][CH3:1])[C:8]([CH3:9])=[CH:7][N:6]=1)=[O:23].[SH:13][C:14]1[NH:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1.[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][N:6]=[C:5]([C:10](=[O:23])[C:31]([O:32][CH3:26])=[O:34])[C:4]=1[CH3:24]

Participants

8

Procedure

To a suspension of 250 mg of 3-[(4-methoxy-3,5-dimethyl-2-pyridyl)oxomethyl]-1,2,4-thiadiazolo[4,5-a]benzimidazole in 125 mL methanol and 38 mL 0.1 M hydrochloric acid was added 161 μL of 3-mercaptopropionic acid. After complete degradation of the starting material, the mixture was neutralized to pH 6 with aqueous sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate was dried on anhydrous magnesium sulfate and evaporated. The crude material was purified by chromatography to give 93 mg of 2-imino-2-(2-mercapto-1-benzimidazolyl)-1-(4-methoxy-3,5-dimethyl-2-pyridyl) ethanone, 65 mg of 2-mercaptobenzimidazole and 61 mg of methyl 2-(4-methoxy-3,5-dimethyl-2-pyridyl)-2-oxoacetate. 2-Imino-2-(2-mercapto-l-benzimidazolyl)-1-(4-methoxy-3,5-dimethyl-2-pyridyl)ethanone: 1H NMR (CDCl) δ 10.55 (br s, 1H, NH or SH), 10.35 (br s, 1H, NH or SH), 8.10 (d, 1H, J=7 Hz, ArH), 7.80 (s, 1H, H6 of pyridyl), 7.35-7.20 (m, 2H, 2×ArH), 7.10 (d, 1H, J=7.9 Hz, ArH), 3.75 (s, 3H, OCH3), 2.60 (s, 3H, ArCH3), 2.15 (s, 3H, ArCH3) ppm; IR (KBr) ν 3262, 1691, 1635, 1502, 1458, 1396, 1328, 1272, 1247, 1004, 746 cm-1 ; MS (electrospray) m/z 341 (MH+), 191 (MH+ -2-mercaptobenzimidazole). 2-Mercaptobenzimidazole: the material was found to be identical to an authentic sample purchased from Aldrich Chemical Co. by 1H NMR, IR and TLC. Methyl 2-(4-methoxy-3,5-dimethyl-2-pyridyl)-2-oxoacetate:

Workup

  1. extractionextracted with ethyl acetate
  2. dry with materialThe ethyl acetate was dried on anhydrous magnesium sulfate
  3. customevaporated
  4. customThe crude material was purified by chromatography

Sources & evidence

ORD record
ord-adc7c598615c4724ac4f07b3ef70d985
Source dataset
uspto-grants-2000_07
Patent number
US06093738

Reaction notes

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