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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842409Generated: October 26, 2026

Sodium borohydride → Imidazo[1,2-b]pyridazin-6-ylmethanol

https://huagongshe.com/reaction/1842409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl imidazo[1,2-b]pyridazine-6-carboxylateHCID 59580147—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductImidazo[1,2-b]pyridazin-6-ylmethanolHCID 5958009981%

Reaction Steps

Sodium borohydride (1.1 g, 31.1 mmol) was added to a solution of methyl imidazo[1,2-b]pyridazine-6-carboxylate (2.4 g, 15.5 mmol) in THF (35 mL) and methanol (2.5 ml) at RT. The reaction mixture was stirred at RT for 2 h (the reaction was monitored by TLC) upon which the mixture was concentrated under reduced pressure. The reaction mixture was diluted with water and extracted with EtOAc. The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to afford imidazo[1,2-b]pyridazin-6-ylmethanol (1.6 g, 81%,) as a white solid. 1H NMR: 200 MHz, DMSO-d6: δ 8.5 (s, 1H), 8.3 (d, 1H), 7.9 (s, 1H), 7.55 (d, 1H), 5.65 (t, 1H), 4.6 (d, 2H). MS: [M+H]+: m/z=311.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946222B2
Source datasetuspto-grants-2015_02
ORD IDord-3f547ab65c9f4668831ffdcccdf51312
Source noteuspto-grants-2015_02