Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873979Generated: October 31, 2026

Triphenylphosphine → HCID 59370744, compound

https://huagongshe.com/reaction/1873979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantCarbonate IonHCID 19660—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 59370757HCID 59370757—
ReactantHCID 135869950HCID 135869950—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 59370744HCID 5937074447.4%

Reaction Steps

(R)-Tert-butyl 2-(3-aminophenyl)-2-(triethylsilyloxy)ethyl(2-hydroxyethyl)carbamate (1.6143 g) which can be prepared according to the method described in Reference example 59, etc. and tert-butyl 6-hydroxy-3-cyclopropylindazole-1-carboxylate (924 mg) which can be prepared according to the method described in Reference example 7, etc. and triphenylphosphine (1.1419 g; manufactured by Kanto Chemical Co., Inc.) were dissolved in dehydrated toluene (18 mL), added with DIAD (808 μL; manufactured by Sigma-Aldrich Co.), and stirred overnight at room temperature. The reaction solution was purified by column chromatography (“COLUMN-A”; n-hexane:ethyl acetate=82:18→61:39) to obtain a crude product (1.669 g), which was then dissolved in CH2Cl2 (20 mL). After adding MP-Carbonate [5.15 g (2.73 mol/g); manufactured by Argonaut] to the mixture, it was stirred overnight at room temperature. After filtering the reaction solution, the filtrate was concentrated under reduced pressure to obtain the title compound (1.0644 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304443B2
Source datasetuspto-grants-2012_11
ORD IDord-a77ae661824d48838369dd7ca0a3e8da
Source noteuspto-grants-2012_11