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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873982Generated: November 3, 2026

Triphenylphosphine → HCID 59370710, compound

https://huagongshe.com/reaction/1873982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN,N-DibenzylethanolamineHCID 22657—
ReactantDiamideHCID 5353800—
ReactantHCID 135869969HCID 135869969—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59370710HCID 5937071088.9%

Reaction Steps

Tert-butyl 3-chloro-6-hydroxyindazole-1-carboxylate (4.3611 g) which can be prepared according to the method described in Reference example 39, etc. and 2-(dibenzylamino)ethanol (4.1529 g; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated THF (100 mL), added with triphenylphosphine (7.9370 g; manufactured by Kanto Chemical Co., Inc.) and TMAD (5.2270 g; manufactured by Masuda Chemical Industries Co., Ltd.), and then stirred overnight at room temperature. The reaction solution was filtered and the filtrate was concentrated under reduced pressure. The resulting residue was dissolved in toluene, and the solvent was evaporated under reduced pressure. The resulting residue was purified by column chromatography (“COLUMN-D”; n-hexane:ethyl acetate=90:10→75:25) to obtain the title compound (7.1028 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304443B2
Source datasetuspto-grants-2012_11
ORD IDord-749e437dbb7a4095aa73970ed5e73eeb
Source noteuspto-grants-2012_11