HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619946Generated: October 30, 2026
Methanesulfonic Acid → HCID 135568536, compound
https://huagongshe.com/reaction/619946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14155248 | HCID 14155248 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 135568536 | HCID 135568536 | 37% |
Reaction Steps
Sodium borohydride (0.6 g, 16 mmol) was added to a solution of 3.0 g (8.3 mmol) of 5-methyl-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide in 25 ml of dry DMSO. An exothermic reaction occured and 2.0 ml (31 mmol) of methanesulfonic acid in 5 ml of DMSO was added at a rate to maintain the temperature of the reaction mixture at 60° C. After the addition was complete the reaction mixture was stirred for 10 minutes and carefully quenched with 0.5N aqueous NaOH. The clear yellow solution was filtered, and the fitrate was acidified with 3N aqueous HCl. The resulting precipitate was treated with dilute aqueous NaOH and filtered to remove insoluble material. The filtrate was acidified with aqueous HCl to precipitate a solid. The solid was collected by filtration and dried to yield 1.11 g (37%) of the desired product as a solid, mp 230°-235° C. IR and 1H NMR spectra were in agreement with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04818273 |
|---|
| Source dataset | uspto-grants-1989_04 |
|---|
| ORD ID | ord-32bcb7283570466c91eca6ff58d0f2a5 |
|---|
| Source note | uspto-grants-1989_04 |
|---|