HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723795Generated: October 30, 2026
1-Chloroethyl chloroformate → HCID 69363543, compound
https://huagongshe.com/reaction/723795
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 69364497 | HCID 69364497 | — |
| Catalyst | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69363543 | HCID 69363543 | 86.7% |
Reaction Steps
1-Chloroethyl chloroformate (1.18 g, 8.3 mM) was added dropwise, under an atmosphere of nitrogen, to a stirred solution of (5R)-3-(4-(1-benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one (2.56 g, 5.90 mM) and N,N-diisopropylethylamine (0.230 mg, 1.77 mM) in dichloromethane (50 ml) with cooling in ice/water. The reaction was stirred for 30 minutes at ice temperature, and the brown solution purified by MPLC on silica, eluting with 75% ethyl acetate in isohexane. The resulting carbamate intermediate was dissolved in methanol (60 ml) and heated at 60° for 30 minutes. Evaporation of the solvent and trituration with diethyl ether gave the title compound (1.76 g) as its hydrochloride salt. MS (ESP): 345 (MH+) for C16H17FN6O2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141583B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-7a33acd654d04ddbb063a5d030dfee22 |
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| Source note | uspto-grants-2006_11 |
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