HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154488Generated: October 31, 2026
Cyclopropanemethanol → HCID 53843677, compound
https://huagongshe.com/reaction/1154488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanemethanol | HCID 75644 | — |
| Reactant | Ethyl (7S)-12-oxo-2,4,11-triazatetracyclo[11.4.0.02,6.07,11]heptadeca-1(17),3,5,13,15-pentaene-5-carboxylate | HCID 10041121 | — |
| Catalyst | Titanium(IV)ethoxide | HCID 2724286 | — |
| Product | HCID 53843677 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04489003 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-d7f1a027811d421382ec88c230e14a51 |
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| Source note | uspto-grants-1984_12 |
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