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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815594Generated: October 31, 2026

Acetyl chloride → HCID 6321073, compound

https://huagongshe.com/reaction/1815594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 6321070HCID 6321070—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductHCID 6321073HCID 632107386%

Reaction Steps

A solution of 21 mg (0.033 mmol) of (3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxy-1-[4-(2-aminoethoxy)benzyl]propylcarbamate in 2 mL of 1:1 THF/CH2Cl2 was treated with 9 μL (0.050 mmol) of N,N-diisopropylethylamine followed by 2.6 μL (0.036 mmol) of acetyl chloride. The resulting solution was stirred at RT. After 1.5 hours the solution was concentrated in vacuo and the residue subjected to flash chromatography (SiO2, 95:5 CH2Cl2/MeOH) to afford the desired compound in 86% yield as a white foam. 1H NMR (CDCl3): 7.29 (dd, 1H), 7.16-7.04 (m, 3H), 7.05 (d, 1H), 6.76 (d, 2H), 6.05 (s, 2H), 5.91 (br s, 1H), 5.01 (d, 1H), 5.05-4.89 (m, 2H), 3.94 (m, 3H), 3.80 (m, 3H), 3.72-3.51 (m, 5H), 3.08 (dd, 1H), 3.01-2.83 (m, 4H), 2.74 (m, 2H), 1.97 (s, 3H), 1.86-1.45 (m, 3H), 0.90 (d, 3H), 0.84 (d, 3H). MS(ESI): 678(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878728B1
Source datasetuspto-grants-2005_04
ORD IDord-f24f0d2ea3244badbb5d2d3240ff370f
Source noteuspto-grants-2005_04