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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154488Generated: October 31, 2026

Cyclopropanemethanol → HCID 53843677, compound

https://huagongshe.com/reaction/1154488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanemethanolHCID 75644—
ReactantEthyl (7S)-12-oxo-2,4,11-triazatetracyclo[11.4.0.02,6.07,11]heptadeca-1(17),3,5,13,15-pentaene-5-carboxylateHCID 10041121—
CatalystTitanium(IV)ethoxideHCID 2724286—
ProductHCID 53843677HCID 53843677—

Reaction Steps

A mixture of 6.22 g (20 mmol) of ethyl (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylate, 1.52 g (6.7 mmol) of tetraethyl orthotitanate and 10 g (194 mmol) of hydroxymethyl-cyclopropane is stirred at 115° overnight, evaporated to dryness, the residue is taken up in methylene chloride and stirred for 0.5 hour with about 50 ml of water. The emulsion obtained is filtered through siliceous earth, the organic phase is washed with saturated sodium bicarbonate solution, dried over magnesium sulphate and evaporated. By recrystallization of the residue from ethyl acetate there is obtained cyclopropylmethyl (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylate of melting point 189-190°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489003
Source datasetuspto-grants-1984_12
ORD IDord-d7f1a027811d421382ec88c230e14a51
Source noteuspto-grants-1984_12