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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094117Generated: November 3, 2026

1H-Benzotriazole-1-methanol → HCID 59257892, compound

https://huagongshe.com/reaction/1094117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Benzotriazole-1-methanolHCID 224169—
ReactantSodium borohydrideHCID 4311764—
Reactant5-amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 59166722—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 59257892HCID 59257892—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (−)-5-amino-1,3-dihydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one (154 mg, 0.613 mmol, described in Intermediate 3) and 1-(hydroxymethyl)benzotriazole (93 mg, 0.625 mmol) in EtOH (2 mL) and DMF (0.2 mL) was heated at reflux for 4 h, then concentrated to dryness under reduced pressure. The residue was resuspended in THF (3 mL) and sodium borohydride (40 mg, 1.05 mmol) was added. The resulting mixture was heated to 70° C. for 6 h then quenched with H2O (50 mL) and extracted with EtOAc (50 mL). The organic extract was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 80:20, to give the title compound, which was of sufficient purity for use in the next step. MS: m/z=266 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133891B2
Source datasetuspto-grants-2012_03
ORD IDord-3dae26b40a6248d3b6e70672ea8f897d
Source noteuspto-grants-2012_03