HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (6-Chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Chloro-2-cyclopropylimidazo[1,2-b]pyridazine-3-carbaldehyde | HCID 57743050 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (6-Chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methanol | HCID 58009731 | 93% |
Reaction Steps
Sodium borohydride (5.62 mg, 6.62 mmol, 1.3 eq) is added dropwised, at room temperature, to a solution of 6-chloro-2-cyclopropylimidazo[1,2-b]pyridazine-3-carbaldehyde x110 (958 mg, 4.32 mmol) in methanol (100 ml). After 1 hour, the reaction is quenched by water (100 ml) and the crude product is extracted by dichloromethane (2×100 ml). The organic layers are dried over MgSO4, filtered and condensed under reduced pressure to afford (6-chloro-2-cyclopropylimidazo[1,2-b]pyridazin-3-yl)methanol x115 which is used without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518943B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-79537ae1afab49f1a0aa40aa28ae613f |
| Source note | uspto-grants-2013_08 |