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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220271Generated: October 30, 2026

Beta-Alanine → HCID 11316614, compound

https://huagongshe.com/reaction/2220271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantTriethylamineHCID 8471—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86596037HCID 86596037—
SolventMethanolHCID 887—
ProductHCID 11316614HCID 1131661436.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-(2-trifluoromethyl-biphenyl-4-yl)-2,3-dihydro-1H-isoindole-5-carbaldehyde (19 mg, 0.05 mmol) in 3 mL MeOH, β-alanine (8.7 mg, 0.1 mmol) and catalytic amount Et3N are added. The suspension is heated to 50° C. for 0.5 hours, followed by adding 2 mg of NaBH4. After pre-LC-MS, 8 mg of 3-{[2-(2-trifluoromethyl-biphenyl-4-yl)-2,3-dihydro-1H-isoindol-5-ylmethyl]-amino}-propionic acid is obtained as a white solid. MS m/z 441[M+1]+. 1H NMR (DMSO-d6): δ 7.08-7.26 (m, 9H), 6.80 (brs, 2H), 4.53 (s, 4H), 3.68 (s, 2H), 2.62 (t, 2H), 2.16 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417065B2
Source datasetuspto-grants-2008_08
ORD IDord-57e21730b0da4512981f81c9ed525586
Source noteuspto-grants-2008_08