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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842586Generated: November 2, 2026

Triethylamine → 2,2-Dimethyl-N-(6-methyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)propanamide

https://huagongshe.com/reaction/1842586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 135797460HCID 135797460—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product2,2-Dimethyl-N-(6-methyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)propanamideHCID 135797453—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a 250-mL round-bottomed flask was added 8 (1.37 g, 8 mmol), suspended in 40 mL of dichloroethane; then trimethylacetyl chloride (1.99 mL, 16 mmol), DMAP (0.13 g, 1 mmol) and triethylamine (2.68 mL) were added. The mixture was stirred overnight at 50° C. The resulting mixture was cooled, diluted with dichloromethane (50 mL), washed with brine (40 mL×2), dried over Na2SO4 and concentrated in vacuo. To this solution were added methylene chloride (30 mL) and silica gel (5 g) and the solvent evaporated. The silica gel plug obtained was loaded onto a silica gel column and eluted with 9:1 ethyl acetate/n-hexane The fractions containing the product (TLC) were pooled and the solvent was evaporated to afford 1.33 g (67%) of9 as a white solid: TLC Rf0.47 (MeOH/CHCl3, 1:10); mp 156-157° C.; 1H NMR (DMSO-d6) δ 1.19 (s, 9 H), 2.29 (s, 3 H), 5.97 (s, 1 H), 10.72 (s, 1 H), 11.78 (s, 1 H), 11.87 (s, 1 H). Anal. (C12H16N4O20.15CH3COCH3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946239B2
Source datasetuspto-grants-2015_02
ORD IDord-afc43d0c8ed942e2b34f15536b79fa49
Source noteuspto-grants-2015_02