HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994397Generated: October 30, 2026
Acetic Acid → 6-(4-Chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-3-dimethylamino-8-isopropylhexahydropyrazino[1,2-a]pyrimidine-4,7-dione
https://huagongshe.com/reaction/1994397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-(4-Chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-3-amino-8-isopropylhexahydropyrazino[1,2-a]pyrimidine-4,7-dione hydrobromide | HCID 68693464 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(4-Chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-3-dimethylamino-8-isopropylhexahydropyrazino[1,2-a]pyrimidine-4,7-dione | HCID 59134211 | — |
Reaction Steps
200 mg of 6-(4-chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-3-amino-8-isopropylhexahydropyrazino[1,2-a]pyrimidine-4,7-dione hydrobromide (Example 2) were dissolved in 15 ml of methanol, and 600 μl of acetic acid were added. 0.5 ml of 37% strength aqueous formaldehyde and 3 ml of 1M sodium cyanoborohydride solution in THF were added to this solution. After 2 hours, the reaction mixture was evaporated, suspended in 5% Et3N in ethyl acetate and filtered through a small silica gel column. The eluent was evaporated, and the crude substance was dissolved in a mixture of acetonitrile and water and freeze dried. The pure title compound was removed after purification by HPLC. The system and process described under “general processes” was used for this. MW=586.10 (calculated, monoisotopic); measured value (M+H)+: 587.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07652007B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-dd8ab89909724d3a9861e42470417e72 |
|---|
| Source note | uspto-grants-2010_01 |
|---|