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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595963Generated: October 30, 2026

Methylamine → HCID 22941792, compound

https://huagongshe.com/reaction/1595963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 22941787HCID 22941787—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22941792HCID 2294179279.8%

Reaction Steps

6.3 g of methylamine is condensed in a pressure pipe while being cooled with ice in a solution of 8.2 g of 17β-acetoxy-3-(tetrahydropyran-2-yloxy)-7α-(5-p-toluenesulfonyloxypentyl)-estra-1,3,5(10)-triene in 80 ml of tetrahydrofuran. The closed pressure pipe is then heated for 6 hours to 60° C. After cooling, it is evaporated to dryness in a vacuum, and the residue is chromatographed on silica gel. 5.1 g of 17β-acetoxy-7α-(5-methylaminopentyl)-3-(tetrahydropyran-2-yloxy)-estra-1,3,5(10)-triene is obtained as an oil. [α]D=+29.7° (c=0.535% in chloroform)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288051B1
Source datasetuspto-grants-2001_09
ORD IDord-0be96c32fadb4d69a4dbde6b80f5249a
Source noteuspto-grants-2001_09