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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656603Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 19788722, compound

https://huagongshe.com/reaction/1656603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-(Methylsulfonamido)benzoic acidHCID 250653—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 19788730HCID 19788730—
SolventDimethylformamideHCID 6228—
ProductHCID 19788722HCID 1978872273%

Reaction Steps

4-(Methylsulfonylamino) benzoic acid (2.16 g, 10.05 mmol) was added to a stirring solution of 1-hydroxybenzotriazole hydrate (1.36 g, 10.05 mmol) and dicyclohexylcarbodiimide (2.08 g 10.05 mmol) in DMF (30 mL) at 25° C. under nitrogen. After 45 minutes, 1-[2-(6-methyl-2-pyridyl)ethyl]piperazine (2.27 g, 11.05 mmol) was added as a suspension in DMF (15 mL). The resulting mixture was stirred at room temperature overnight. The work-up was performed as disclosed in Example 5 to give 2.94 g (73%) of the title compound which was treated with ethanolic HCl to afford 2.15 g of product as a dihydrochloride: mp 165°-167° C.; 1H NMR (DMSO-d6): δ 10.14 (s, 1H), 8.19 (m, 1H), 7.63 (m, 2H), 7.45 (d, J=8.72 Hz, 2H), 7.25 (d, J=8.71 Hz, 2H), 3.85-3.20 (m, 12H), 3.06 (s, 3H), 2.67 (s, 3H); IR (KBr): 3420, 3000, 2560, 1640 cm-1 ; MS (m/z) 403 (MH+, 25%) 217 (30), 91 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254689
Source datasetuspto-grants-1993_10
ORD IDord-2b236c55a84a45589a106111a2f4a188
Source noteuspto-grants-1993_10