Methanol → HCID 178491901, compound

HRID 370118Notes

Reaction equation

HRID 370118 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:35])[C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([O:17][CH3:18])[C:11]=2[NH:19][C:20]([C:22]2[S:23][CH:24]=[C:25]([CH2:28][N:29]3[CH:33]=[CH:32][N:31]=[C:30]3[NH2:34])[C:26]=2[Cl:27])=[O:21])=[N:6][CH:7]=1.S(=O)(=O)(O)O.ClN1[C:46](=[O:47])CCC1=O.[OH2:49].[CH3:50]O>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:35])[C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([O:17][CH3:18])[C:11]=2[NH:19][C:20]([C:22]2[S:23][CH:24]=[C:25]([CH2:28][N:29]3[C@H:33]([O:47][CH3:46])[C@H:32]([O:49][CH3:50])[NH:31][C:30]3=[NH:34])[C:26]=2[Cl:27])=[O:21])=[N:6][CH:7]=1

Participants

6

Reactant 5

HCID 887MethanolHCID 962WaterHCID 1118Sulfuric AcidHCID 31398ChlorosuccinimideHCID 167330134-[(2-amino-1H-imidazol-1-yl)methyl]-3-chloro-N-{4-chloro-2-[(5-chloropyridin-2-yl)carbamoyl]-6-methoxyphenyl}thiophene-2-carboxamide

Product 1

HCID 178491901HCID 178491901, compound

Procedure

N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide (0.053 g, 0.96 mmol) and sulfuric acid (0.10 g, 1.06 mmol) in methanol (10 mL) was added N-chlorosuccinimide (0.192 g, 1.43 mmol). After stirring at ambient temperature for 6 hours, the reaction was poured into water and extracted with ethyl acetate. The ethyl acetate extract was dried over sodium sulfate, concentrated in vacuo, and purified by flash chromatography on silica gel to give 0.33 g of N-(5-chloropyridin-2-yl)-2-[((4-((cis4,5-dimethoxy-2-iminotetrahydroimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide; NMR (CDCl3) 9.0 (d, 2), 8.3 (d, 1), 8.1 (d, 1), 7.7 (dd, 1), 7.5 (s, 1), 7.3 (d, 1), 7.1 (d, 1), 6.0 (brs, 1), 4.8 (m, 2), 4.6 (d, 1), 4.3 (d, 1), 3.9 (s, 3), 3.4 (s, 3), 3.3 (s, 3) ppm.

Workup

  1. extractionextracted with ethyl acetate
  2. extractionThe ethyl acetate extract
  3. dry with materialwas dried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. custompurified by flash chromatography on silica gel

Sources & evidence

ORD record
ord-505de881d1ec4333bd0bfb2d851b1c3a
Source dataset
uspto-grants-2000_10
Patent number
US06140351

Reaction notes

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