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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870612Generated: November 2, 2026

N-((1,1-dimethylethoxy)carbonyl)-beta-alanine → HCID 86726577, compound

https://huagongshe.com/reaction/870612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-(indan-2-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amineHCID 86726522—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86726577HCID 8672657783.4%

Reaction Steps

Add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.69 g; 1.5 equiv; 14.06 mmoles) to a flask containing 3-(tert-butoxycarbonylamino)propanoic acid (1.8 g; 1.0 equiv; 9.37 mmoles), N-indan-2-yl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amine (2.50 g; 1.0 equiv; 9.37 mmoles) and N,N-dimethyl-4-pyridinamine, (0.229 g; 0.2 equiv; 1.87 mmoles) in dichloromethane (30 mL). Stir the mixture for 2 hours, then load the solution directly onto a silica gel column and purify by column chromatography (30 to 100% ethyl acetate in dichloromethane) to give tert-butyl {3-[2-(2,3-dihydro-1H-inden-2-ylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl]-3-oxopropyl}carbamate (3.42 g; 83%) as a colorless foam: MS (m/z): 438(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969555B2
Source datasetuspto-grants-2015_03
ORD IDord-04674558fb404e269e003f07ddec21b9
Source noteuspto-grants-2015_03