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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51185Generated: October 24, 2026

Dichloromethane → N-(Carbamoylmethyl)-N-(thymin-1-ylacetyl)-beta-alanine ethyl ester

https://huagongshe.com/en/reaction/51185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(5-Methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)acetic acidHCID 853753—
ReactantN-(Carbamoylmethyl)-beta-alanine ethylesterHCID 22737577—
SolventDimethylformamideHCID 6228—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
ProductN-(Carbamoylmethyl)-N-(thymin-1-ylacetyl)-beta-alanine ethyl esterHCID 2273756961.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

DhbtOH (9.37 g, 57.4 mmol), N1-thyminyl acetic acid (10.57 g, 57.4 mmol) and CH2Cl2 (100 mL) were added to a solution of N-(carbamoylmethyl)-β-alanine ethylester (10.0 g, 57.4 mmol) in dry DMF (100 mL). The solution was cooled to 0° C. in an ice bath and a solution of DCC (1.90 g, 9.18 mmol) in DMF/CH2Cl2 (100 mL, 1:1 v/v) was added dropwise within 20 minutes. The ice bath was removed and after stirring for 1 hour at room temperature. The reaction mixture was filtered and the precipitate (DCU) was rinsed with CH2Cl2 (50 mL). The organic solution and the CH2Cl2 rinse were combined. A colorless precipitate formed overnight which was filtered and rinsed with CH2Cl2. The precipitate was dried in vacuo to give 12.0 g (61%) (mp 207-208° C.) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713602B1
Source datasetuspto-grants-2004_03
ORD IDord-e79c5c77798049f2af95b4ccefdf6e6b
Source noteuspto-grants-2004_03