HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660064Generated: October 31, 2026
Isobutylamine → N-(isobutyl)-2-(2-(phenylsulfonyl)ethylthio)nicotinamide
https://huagongshe.com/reaction/660064
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-[2-(Phenylsulfonyl)ethylthio]nicotinic acid | HCID 2821350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(isobutyl)-2-(2-(phenylsulfonyl)ethylthio)nicotinamide | HCID 68745486 | — |
Reaction Steps
171 mg (1.05 mmol) of CDI were added to a solution of 323 mg (1.00 mmol) of 2-(2-(phenylsulfonyl)ethylthio)nicotinic acid in DCM (16 ml), and the mixture was stirred for 1 hour at RT. 99 μl (1.00 mmol) of isobutylamine were then added, and stirring was continued for a further 5 days at RT. The reaction solution was then washed in each case twice with a 4 M aq. ammonium chloride solution and a 1 M aq. sodium hydrogen carbonate solution. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The residue obtained was taken up in ethyl acetate (30 ml) and washed with 0.4 M hydrochloric acid (5 ml). The organic phase was again dried over MgSO4, filtered and concentrated in vacuo. 160 mg (0.42 mmol, 42 of N-(isobutyl)-2-(2-(phenylsulfonyl)ethylthio)nicotinamide were obtained as residue. MS: m/z 379.1 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084470B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-376cee0168bb47cf8449a3967450de1e |
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| Source note | uspto-grants-2011_12 |
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