HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411288Generated: October 31, 2026
Dimethylamine, hydrochloride → HCID 9851312, compound
https://huagongshe.com/reaction/411288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 9893934 | HCID 9893934 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 9851312 | HCID 9851312 | — |
Reaction Steps
A mixture of 1-undecyl-2-(4-fluorobenzyl)thio-5-(1-(carboxymethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin-4-one, dimethylamine hydrochloride (0.02 g), diisopropylethylamine (0.045 ml), hydroxybenzotriazole (0.005 g) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.045 g) in dry methylene chloride were stirred together for 24 h and diluted with 3% methanol in methylene chloride and 5% aqueous potassium carbonate. The organic layer was added directly to a SepPak cartridge (SiO2, 10 g) and eluted with 0-20% methanol in ethyl acetate to give the desired product (0.085 g). 1H-NMR (CDCl3) δ0.8-0.95 (3H,m), 1.15-1.4 (16H,m), 1.6-1.85 (2H,m), 2.98 (3H,s), 3.13 (3H,s), 3.49 (2H,s), 3.77 (2H,t), 4.46 (2H,s), 4.74 (2H,s), 6.9-7.1 (2H,m), 7.14 (1H,s), 7.3-7.45 (2H,m), 7.78 (1H,bd), 8.49 (1H,bd); MS (APCI+) found (M+1)=584; C31H42FN5O3S requires 583.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559155B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-a75b1b6d87a94f42a194c6dde09ef78d |
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| Source note | uspto-grants-2003_05 |
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