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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074967Generated: October 30, 2026

Methyl chloroformate → HCID 480403, compound

https://huagongshe.com/reaction/2074967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 480397HCID 480397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 480403HCID 48040398.5%

Reaction Steps

A solution of 50 mg (0.081 mmol) of (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl N-[(1S,2R)-3-((5-amino-2,2-dimethylpentyl)[3-(methylamino)phenyl]sulfonylamino)-1-benzyl-2-hydroxypropyl]carbamate and 17 μL (0.097 mmol) of N,N-diisopropylethylamine in 4 mL of anhydrous THF at 0° C. was treated with 6.9 μL (0.089 mmol) of methyl chloroformate. The solution was allowed to warm to RT with stirring. After 18 hours the solution was concentrated in vacuo and the residue was subjected to flash chromatography (SiO2, 95:5 CH2Cl2/2M NH3 in MeOH) to afford 54 mg (98%) of the desired compound as a white foam. H1-NMR (CDCl3): 7.28 (m, 6H), 6.99 (d, 1H), 6.89 (s, 1H), 6.71 (dd, 1H), 5.54 (d, 1H), 5.30 (d, 1H), 4.93 (m, 2H), 4.17-3.50 (m, 11H), 3.25-2.60 (m, 12H), 1.60-1.12 (m, 6H), 0.89 (s, 3H), 0.81 (s, 3H). MS(ESI): 677(M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919523B2
Source datasetuspto-grants-2011_04
ORD IDord-3b53d3b4e7ca476a972e24ee593080ed
Source noteuspto-grants-2011_04