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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743239Generated: October 31, 2026

Trimethylsilyldiazomethane → HCID 69795109, compound

https://huagongshe.com/reaction/1743239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 67136426HCID 67136426—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
ProductHCID 69795109HCID 69795109—

Reaction Steps

A total of 1.5 ml of a 2 molar solution of trimethylsilyldiazomethane in hexane is added in portions to a solution of 250 mg of (3R,6R,7aS)-6-benzyl-6-tert-butoxycarbonylamino-5-oxohexahydropyrrolo[2,1-b]thiazole-3-carboxylic acid in 8 ml of methanol while stirring at room temperature. After the reaction is complete, the excess trimethylsilyldiazomethane is destroyed by dropwise addition of glacial acetic acid, and the volatile constituents are stripped off in a rotary evaporator at 40° C. The residue is purified on a column (silica gel, mobile phase:ethyl acetate:n-heptane=1:1.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008957B2
Source datasetuspto-grants-2006_03
ORD IDord-e1458947829447c7a67df207ccaa5a4b
Source noteuspto-grants-2006_03