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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455152Generated: October 29, 2026

1,2-Dichloroethane → HCID 69018289, compound

https://huagongshe.com/reaction/1455152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthylamineHCID 6341—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 21076923HCID 21076923—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69018289HCID 6901828953%

Reaction Steps

To a solution of 1-benzyl-2-{(R)-[(3-tert-butoxycarbonylamino-propyl)-(1-p-tolyl-methanoyl)-amino]-methyl-propyl}-4-methyl-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid (100 mg, 0.169 mmol) in CH2Cl2 (1.7 mL) was added EDC (36 mg, 0.186 mmol), HOBt (25 mg, 0.186 mmol), TEA (28 uL, 0.203 mmol) followed by ethylamine (85 uL of a 2.0M solution in THF, 0.169 mmol). The reaction mixture was stirred at ambient temperature for 16 h, then TFA (1 mL) was added. After 3 h, the reaction mixture was concentrated under reduced pressure and the residue was purified by reverse phase HPLC to give 47 mg (53%) of 2-{(R)-[(3-amino-propyl)-(1-p-tolyl-methanoyl)-amino]-methyl-propyl}-1-benzyl-4-methyl-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethylamide as a pale yellow solid: MS (ES) m/e 518.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482343B2
Source datasetuspto-grants-2009_01
ORD IDord-65545e0b463f41a8a2d542a927ee75c9
Source noteuspto-grants-2009_01