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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359713Generated: October 29, 2026

Pivaloyl chloride → 2-(4-Trimethylacetylthiophenyl)3-(4-pyridyl)-6,7-dihydro [5H]-pyrrolo[1,2 a]imidazole

https://huagongshe.com/reaction/359713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant(4-mercaptophenyl) 3 (4-pyridyl) 6,7dihydro[5H]-pyrrolo[1,2-a]imidazoleHCID 135962046—
SolventDichloromethaneHCID 6344—
Product2-(4-Trimethylacetylthiophenyl)3-(4-pyridyl)-6,7-dihydro [5H]-pyrrolo[1,2 a]imidazoleHCID 1987921733.5%

Reaction Steps

To 1.0 q (3.4 mmole) of 2-(4 mercaptophenyl)-3-(4-pyridyl)-6,7-dihydro [5H]pyrrolo[1,2-a]imidazole prepared as in Example 16 in 50ml methylene chloride at ° C. was added a solution of 0.3 q (3.7 mmole, 0.26 ml) trimethylacetyl chloride in 10 ml CH2Cl2 over a period of 10 minutes. The reaction was allowed to come to room temperature and was stirred for 30 minutes. The mixture was then diluted with methylene chloride and washed with N NaHCO3, saturated NaCl, treated with Na2SO4, stripped, then flash chromatographed on silica with methylene chloride containing 1% to 5% MeOH. The isolated material was recrystallized from ethyl acetate to give 0.43 g of the titled compound. 33.5% yield, mp 216-217.5 ° C. C22H23N3OS, Calculated, C: 70.00, H: 6.14, N: 1.13; Found, C: 70.01, H: 6.20, N: 10.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002941
Source datasetuspto-grants-1991_03
ORD IDord-0df4002140ad4ab19a503659080bc73b
Source noteuspto-grants-1991_03