Butyryl chloride → HCID 53878971, compound

HRID 1389773Notes

Reaction equation

[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][CH2:10][CH2:11][N:12]1[CH2:17][CH2:16][CH:15]([N:18]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:19](=[O:22])[CH2:20][CH3:21])[CH2:14][CH2:13]1.[C:29](Cl)(=[O:33])[CH2:30][CH2:31][CH3:32]>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]([CH2:10][CH2:11][N:12]1[CH2:13][CH2:14][CH:15]([N:18]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:19](=[O:22])[CH2:20][CH3:21])[CH2:16][CH2:17]1)[C:29](=[O:33])[CH2:30][CH2:31][CH3:32]

Participants

Reactant 2

HCID 8855Butyryl chloride

HCID 20295517HCID 20295517, compound

Product 1

HCID 53878971HCID 53878971, compound

Procedure

Using the same procedure but starting from 1-[2-(2,6-dimethyl phenylamino)-ethyl]-4-(N-phenyl N-propionylamino) piperidine and butyroyl chloride, 1-[2-(N-(2,6-dimethyl phenyl) N-butyrylamino)-ethyl]-4-(N-phenyl N-propionylamino) piperidine is produced.

Sources & evidence

ORD record: ord-609ad50ace5d48188d4e7e152f652dc0
Source dataset: uspto-grants-1981_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04246267

Reaction notes

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