Thionyl Chloride → HCID 18426175, compound

HRID 133622Notes

Reaction equation

[C:1]([C:4]1[CH:34]=[CH:33][C:7]([CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([CH2:15][NH:16][C:17](=[O:32])[CH2:18][NH:19][C:20](=[O:31])[C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:29])[F:28])[CH:22]=3)[CH2:11][CH2:10]2)=[CH:6][CH:5]=1)(O)=[O:2].S(Cl)([Cl:37])=O>>[Cl:37][C:1]([C:4]1[CH:34]=[CH:33][C:7]([CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([CH2:15][NH:16][C:17](=[O:32])[CH2:18][NH:19][C:20](=[O:31])[C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:29])[F:28])[CH:22]=3)[CH2:11][CH2:10]2)=[CH:6][CH:5]=1)=[O:2]

Participants

Reactant 2

HCID 24386Thionyl Chloride

HCID 18426279HCID 18426279, compound

Product 1

HCID 18426175HCID 18426175, compound

Procedure

A mixture of 1-(4-carboxybenzyl)-4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine (240 mg) with thionyl chloride (1 mL) was stirred at room temperature for 12 hours, and the excess thionyl chloride was removed under reduced pressure to thereby afford 1-[4-(chloroformyl)benzyl]-4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine. The resulting acid chloride was used without being further purified.

Workup

customthe excess thionyl chloride was removed under reduced pressure to thereby afford 1-[4-(chloroformyl)benzyl]-4-[[N-(3-(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine

Sources & evidence

ORD record: ord-8b14f848c45744bdb64dd9dd5ecc0386
Source dataset: uspto-grants-2008_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07390830B1

Reaction notes

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