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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805369Generated: November 2, 2026

N-(3-Aminopropyl)morpholine → HCID 67233484, compound

https://huagongshe.com/reaction/1805369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
ReactantMethyl 3-(bromomethyl)benzoateHCID 517981—
Reactant(1S,2R)-2-(4-chlorophenyl)spiro[cyclopropane-1,3'-indolin]-2'-oneHCID 58305285—
ProductHCID 67233484HCID 67233484—

Reaction Steps

The title compound was prepared in analogy to Example 60 starting from form 3 3-morpholinopropan-1-amine, 3-bromomethyl-benzoic acid methyl ester (commercially available), (1R,2S) and (1S,2R)-2-(4-chlorophenyl)spiro[cyclopropane-1,3′-indolin]-2′-one prepared as in Scheme 1. LC/MS m/e calcd. for C31H32ClN3O3: 529, observed (M+H)+: 530.2 1H NMR (400 MHz, MeOD-d4) δppm 2.02-2.15 (m, 2 H) 2.24 (d, J=8.59 Hz, 2 H) 3.15 (br. s., 2 H) 3.23 (d, J=8.08 Hz, 2 H) 3.25-3.31 (m, 1 H) 3.47-3.57 (m, 4 H) 3.79 (t, J=12.38 Hz, 2 H) 4.06 (br. s., 2 H) 5.14 (s, 2 H) 6.09 (d, J=7.33 Hz, 1 H) 6.73 (t, J=7.58 Hz, 1 H) 6.91 (d, J=8.08 Hz, 1 H) 7.09 (t, J=7.71 Hz, 1 H) 7.20-7.28 (m, 2 H) 7.28-7.37 (m, 2 H) 7.49 (t, J=7.71 Hz, 1 H) 7.53-7.61 (m, 1 H) 7.78 (d, J=8.08 Hz, 1 H) 7.87 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354443B2
Source datasetuspto-grants-2013_01
ORD IDord-3f3475ce1bc8419eaff76d34b30e518d
Source noteuspto-grants-2013_01