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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401154Generated: October 30, 2026

Trimethylsilyldiazomethane → HCID 86684745, compound

https://huagongshe.com/reaction/2401154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 86684746HCID 86684746—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86684745HCID 86684745—

Reaction Steps

TMS-Diazomethane (2 M in hexanes, 0.15 mL, 0.300 mmol) was added to a stirred solution of 2-[1-[6-[4-[2-[[(3R,3aR,6R,6aR)-3-hydroxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-6-yl]oxy]-6-chloro-1-(2-trimethylsilylethoxymethyl)-imidazo[4,5-b]pyridin-5-yl]phenyl]-3-pyridyl]pyrazol-4-yl]acetic acid (27.3 mg, 0.039 mmol) in MeOH (0.5 mL) and DCM (0.5 mL). The reaction mixture was stirred at room temperature. After 3.5 hours, the reaction mixture was evaporated under reduced pressure to give the desired compound as a yellow residue. This material was used in the next step without further purification. LC-MS: calculated for C35H39ClN6O7Si 718.23 observed m/e: 719.31 (M+H)+ (Rt 1.26/2 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796258B2
Source datasetuspto-grants-2014_08
ORD IDord-9f9bcfed3a9145cb9f962f58e8e2de92
Source noteuspto-grants-2014_08