HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(Diaminomethyleneamino)-4-(5-hydroxymethylpyridin-3-yl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(Diaminomethyleneamino)-4-(5-methoxycarbonylpyridin-3-yl)thiazole | HCID 10468734 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Diaminomethyleneamino)-4-(5-hydroxymethylpyridin-3-yl)thiazole | HCID 10060619 | 45.3% |
Reaction Steps
A solution of sodium borohydride (1.2 g) in water (25 ml) was added slowly to a solution of 2-(diaminomethyleneamino)-4-(5-methoxycarbonylpyridin-3-yl)thiazole (2.8 g) in methanol (70 ml) and tetrahydrofuran (70 ml) under refluxing for 20 minutes. The mixture was refluxed for 4 hours. The solvent was removed under reduced pressure and the residue was dissolved in water (100 ml). The mixture was extracted with a mixture of ethyl acetate (300 ml) and tetrahydrofuran (150 ml). The extract was dried with magnesium acetate and then evaporated to afford 2-(diaminomethyleneamino)-4-(5-hydroxymethylpyridin-3-yl)thiazole (1.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371097 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-edf8187e6ae346f6bb01e378927aa302 |
| Source note | uspto-grants-1994_12 |