Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356767Generated: October 30, 2026

Dimethylformamide → HCID 18655619, compound

https://huagongshe.com/reaction/356767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 18655613HCID 18655613—
SolventWaterHCID 962—
ProductHCID 18655619HCID 1865561972%

Reaction Steps

A solution of 200 mg (0.34 mmol) of the resultant compound of Example 141 and 98.4 μl (0.75 mmol) of triethylamine in 4 ml of dimethylformamide was treated with 68.0 μl (0.72 mmol) of acetic anhydride. After being stirred at ambient temperature for 2 h, the solution was diluted with water and extracted with four 10 ml portions of 10% methanol in dichloromethane. The combined organic layers were dried over MgSO4, and concentrated in vacuo. Silica gel chromatography of the residue using 10% methanol in dichloromethane provided 164.1 mg (72%) of the desired compound as a white solid. 1H NMR (DMSO-d6) δ 0.69-0.81 (four d, 12H), 1.76 (m, 1H), 1.84 (two s, 6H), 1.92 (m, 1H), 2.60 (dd, 2H), 2.74 (br d, 2H), 2.97 (dd, 1H), 3.67 (d, 2H), 3.72 (d, 2H), 3.85 (m, 1H), 4.02 (m, 2H), 4.17 (dd, 1H), 5.24 (d, 1H), 7.07-7.26 (m, 10H), 7.46(br d, 1H), 7.53 (br d, 1H), 7.56 (br d, 1H), 7.72(br d, 1H), 8.07 (br t, 1H), 8.12 (br t, 1H). Mass spectrum: (M+H)+ =667.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837873
Source datasetuspto-grants-1998_11
ORD IDord-1d3d40f3cacd4e87abd74437bd6d5438
Source noteuspto-grants-1998_11