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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452255Generated: October 29, 2026

1-Naphthaleneacetic Acid → HCID 44132436, compound

https://huagongshe.com/reaction/452255

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthaleneacetic AcidHCID 6862—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ProductHCID 44132436HCID 44132436—

Reaction Steps

The title compound was prepared from Intermediate 10 (200 mg, 0.761 mmol) and 1-naphthylacetic acid (171 mg, 0.913 mmol) in presence of EDCI.HCl (221 mg, 1.141 mmol), HOBt (176 mg, 1.141 mmol) and triethylamine (317 μl, 2.283 mmol) in THF (5 ml) as described in Example 1 to give 250 mg of the product as a white solid; IR (KBr) 3236, 2945, 1638, 1412, 1223, 788 cm−1; 1H NMR (300 MHz, CDCl3) δ 1.47-1.55 (m, 2H), 1.72-1.78 (m, 2H), 2.09 (t, J=7.8 Hz, 3H), 2.16-2.26 (m, 1H), 4.09 (q, J=6.9 Hz, 2H), 5.11-5.19 (m, 1H), 5.29 (d, J=8.4 Hz, 1H), 6.55 (s, 2H), 6.66 (s, 1H), 7.35-7.42 (m, 2H), 7.49-7.59 (m, 2H), 7.77 (d, J=7.2 Hz, 1H), 7.82 (d, J=7.8 Hz, 1H), 7.98 (d, J=7.8 Hz, 1H); APCI-MS (m/z) 392.12 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487121B2
Source datasetuspto-grants-2013_07
ORD IDord-df619f6e69e340348f58c753e1ddee78
Source noteuspto-grants-2013_07