HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76370Generated: October 29, 2026
Hydrochloric Acid → HCID 23650960, compound
https://huagongshe.com/reaction/76370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 4-Fluoro-3-methylbenzene-1,2-diamine | HCID 22055547 | — |
| Reactant | 4-Methyl-2-((3-(1-methylpiperidin-4-yl)propyl)amino)pyrimidine-5-carbaldehyde | HCID 46221560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23650960 | HCID 23650960 | — |
Reaction Steps
To a 2 L Erlenmeyer flask were added 4-fluoro-3-methyl-benzene-1,2-diamine.HCl (46.32 g, 262.3 mmol), Na2S2O5 (64.82 g, 341.0 mmol), and 4-methyl-2-[3-(1-methyl-piperidin-4-yl)-propylamino]-pyrimidine-5-carbaldehyde (72.5 g, 262.3 mmol) in DMF (725 mL). To the resultant mixture was then added triethylamine (36.6 mL, 262.3 mmol), and the reaction was warmed on a hot plate with stirring to 90° C. and held at this temperature for 2 hours. The resultant mixture was then concentrated to near dryness and partitioned between dichloromethane (1 L) and 1 N NaOH (1 L). After separation of the layers, the aqueous layer was extracted a second time with dichloromethane (1 L). The combined organic layers were then washed with saturated aqueous NaHCO3 (1.6 L). The organics were then extracted with a 1 M mono/dibasic phosphate buffer (pH 5.62, 1.23 L). The aqueous layer was then basified with 50% NaOH (80 mL) to pH 10.8. The resultant heterogeneous layer was then extracted with dichloromethane (1.5 L and 500 mL), and the combined organics were concentrated to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08835633B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-f76572d9538c405aade718cd1ea1ee32 |
|---|
| Source note | uspto-grants-2014_09 |
|---|