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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952231Generated: November 2, 2026

Sodium borohydride → (1-Boc-6-fluoro-5-indazolyl)methanol

https://huagongshe.com/reaction/1952231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59490926HCID 59490926—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(1-Boc-6-fluoro-5-indazolyl)methanolHCID 5949088184.1%

Reaction Steps

A solution of tert-butyl 6-fluoro-5-formyl-1H-indazole-1-carboxylate (22E, 3.55 g, 13.4 mmol) in methanol (50.00 mL) was treated with NaBH4 (1.02 g, 26.9 mmol) at 0° C. and stirred for 1 h. The reaction mixture was diluted with water and EtOAc (500 mL). The organic layer was separated and washed with aq. HCl (1M, 200 mL), aq. NaOH (1M, 200 mL) brine (200 mL) dried (MgSO4), filtered, concentrated in vacuo and residue was purified by chromatography (SiO2, EtOAc/hexanes) to yield tert-butyl 5-(hydroxymethyl)-6-fluoro-1H-indazole-1-carboxylate (22F, 3.00 g; Yield=83.9%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404845B2
Source datasetuspto-grants-2013_03
ORD IDord-fb2669b3086f4bd684b9b473acca9caa
Source noteuspto-grants-2013_03