HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064315Generated: November 2, 2026
Diethylmethylamine → HCID 22273523, compound
https://huagongshe.com/reaction/1064315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylmethylamine | HCID 12022 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Reactant | HCID 22273557 | HCID 22273557 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22273523 | HCID 22273523 | 79% |
Reaction Steps
Chlorosulphonic acid (150 μl, 2.16 mmol) was added dropwise to a solution of 2-anilino-4-(1-ethyl-2-methylimidazol-5-yl)pyrimidine (Example 28; 150 mg, 0.54 mmol) in thionyl chloride (3 ml) cooled to 0° C. and the mixture stirred for 10 minutes at 0° C. then heated at 90° C. for 90 minutes. The volatiles were removed by evaporation and the resultant solid placed under high vacuum (<2 mmHg) for 1 hr. The resulting solid was placed under nitrogen and a solution of 2-(2-aminoethyl)ethanol (114 mg, 1.00 mmol) and diethylmethylamine in MeOH (3 ml) was cautiously added. The solution was stirred for 30 minutes and the volatiles were evaporated. Water (20 ml) was added and the precipitated solid was collected by filtration and washed with water (2×10 ml). The residue was dissolved in MeOH (5 ml) and loaded on to an Isolute amine column, eluted with MeOH (30 ml) and the fractions containing product were evaporated to give the title compound (190 mg, 79%) as a beige solid. NMR 1.18 (t, 3H), 2.39 (s, 3H), 2.89 (t, 2H), 3.15 (m, 7H), 4.38 (q, 2H), 7.21 (d, 1H), 7.71 (m, 3H), 7.89 (d, 2H), 8.41 (d, 1H), 9.82 (s, 1H); m/z 447.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06969714B2 |
|---|
| Source dataset | uspto-grants-2005_11 |
|---|
| ORD ID | ord-e8bfac32f8564dd0aaaf6c8950cb0a15 |
|---|
| Source note | uspto-grants-2005_11 |
|---|