HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → HCID 21256484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 54083443 | HCID 54083443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21256484 | HCID 21256484 | 78.3% |
Reaction Steps
A solution of 6,7,8,9-Tetrahydro-5H-cyclohept[d]imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (Formula G-4)(11.7 g) in THF (50 mL) was treated with LiAlH4 (2.24 g) at 0° and reacted at ambient temperature for 1.5 hours. The reaction was quenched by serial additions of water and 15% sodium hydroxide. The mixture was filtered and the filtrate was evaporated to yield crude 6,7,8,9-Tetrahydro-5H-cyclohept[d]imidazo[2,1-b]thiazole-3-methanol (Formula G-5). Crystallization of crude 6,7,8,9-Tetrahydro-5H-cyclohept[d]imidazo[2,1-b]thiazole-3-methanol (Formula G-5) from iso-propanol solution gave pure 6,7,8,9-Tetrahydro-5H-cyclohept [d]imidazo[2,1-b]thiazole-3-methanol (Formula G-5) (7.7 g) m.p. 145-146°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191124B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-9aef184b0f754d838d3fa680459af5bf |
| Source note | uspto-grants-2001_02 |