Hydrochloric Acid → HCID 18412414, compound

HRID 2288374Notes

Reaction equation

HRID 2288374 reaction equation
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]3[CH2:18][CH2:17][CH2:16][CH2:15]3)(=[O:13])=[O:12])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:19][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27]#[N:28])[CH:22]=1.[ClH:29].C(=O)([O-])[O-].[NH4+:34].[NH4+]>C(O)C>[ClH:29].[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]3[CH2:15][CH2:16][CH2:17][CH2:18]3)(=[O:12])=[O:13])=[CH:10][C:5]=2[N:4]=[C:3]1[CH2:19][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27](=[NH:34])[NH2:28])[CH:22]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 517111Ammonium CarbonateHCID 18412506HCID 18412506, compound

Product 1

HCID 18412414HCID 18412414, compoundYield 71%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Prepared analogously to Example 32 from 1-methyl-2-[(3-cyanophenyl)oxymethyl]-benzimidazol-5-yl-sulphonic acid-pyrrolidide, ethanolic hydrochloric acid, ethanol and ammonium carbonate. Yield: 71% of theory, C20H23N5O3S (413.5) EKA mass spectrum: (M+H)+ =414

Sources & evidence

ORD record
ord-f2c74b62882a42bfa7802beb7a79cd3b
Source dataset
uspto-grants-2000_07
Patent number
US06087380

Reaction notes

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