Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | HCID 20602943 | HCID 20602943 | — |
| Reactant | HCID 87874355 | HCID 87874355 | — |
| Product | Adenosylhomocysteine | HCID 439155 | — |
Reaction Steps
L-Homocysteine sodium salt solution (850 Kg), prepared as described above, was cooled to 10° C. and dil.hydrochloric acid (1:1; 100 Lit) was added til the pH became 11.3 to 11.5. To this solution, 5′-Chloromethyl adenosine hydrochloride (135 Kg) and potassium iodide (13.5 Kg) were added and stirred at 70-80° C. for 5 h. The reaction was monitored by HPLC and cooled to 15° C. Dil.hydrochloric acid (1:1; 200 Lit) was added to bring down the pH to 2.0. Activated carbon (10 Kg) was added, stirred for 30 min and filtered. To the mother liquor, ammonia solution (15%) was added to set the pH to 6.0-6.2. The precipitate was stirred at 20° C. for 24 h and filtered. The solid was washed two times with water (200 Lit). The wet cake was dried at 40° C. under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06881837B2 |
|---|
| Source dataset | uspto-grants-2005_04 |
|---|
| ORD ID | ord-d5a1a4f1409d4e788a581ba2cdbddb11 |
|---|
| Source note | uspto-grants-2005_04 |
|---|