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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564390Generated: October 31, 2026

Benzoyl chloride, 3,4-dichloro- → HCID 67004347, compound

https://huagongshe.com/reaction/564390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantHCID 57814014HCID 57814014—
ProductHCID 67004347HCID 67004347—
ProductHCID 67004917HCID 67004917—

Reaction Steps

The title compound was synthesized in similar fashion to 3,4-dichloro-N-[2-({(3R)-1-[1-(4-methoxyphenyl)piperidin-4-yl]pyrrolidin-3-yl}amino)-2-oxoethyl)benzamide, substituting 3-(trifluoromethoxy)benzoyl chloride for 3,4-dichlorobenzoylchloride, as well as 2-amino-N-[(3R)-1-(tetrahydro-2H-pyran-4-yl)pyrrolidin-3-yl]acetamide for 2-amino-N-{(3R)-1-[1-(4-methoxyphenyl)piperidin-4-yl]pyrrolidin-3-yl}acetamide, and was isolated as a white solid. 1H-NMR (CDCl3) δ: 1.40-1.78 (m, 5H), 2.12-2.36 (m, 3H), 2.62 (d, J=5.4 Hz, 2H), 2.83 (m, 1H), 2.94 (m, 1H), 3.33 (m, 2H), 3.91 (m, 2H), 4.06 (d, J=5.4 Hz, 2H), 4.39 (m, 1H), 7.16 (d, J=7.8 Hz, 1H), 7.30 (m, 1H), 7.40 (t, J=8.0 Hz, 1H), 7.70 (m, 1H). MS m/z: 416 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067457B2
Source datasetuspto-grants-2011_11
ORD IDord-6f8a08d9e1914ca180d9c4f1c4f66f5d
Source noteuspto-grants-2011_11