HCID 21465113, compound → HCID 21465123, compound

HRID 1939944Notes

Reaction equation

HRID 1939944 reaction equation
ClCCC(C1C=CC2[NH:10]COC=2C=1)=O.F[C:16]1[CH:42]=[CH:41][C:19]([CH2:20][CH:21]2[CH2:26][CH2:25][N:24]([CH2:27][CH2:28][C:29]([C:31]3[CH:40]=[CH:39][C:34]4[NH:35][C:36](=O)[O:37][C:33]=4[CH:32]=3)=[O:30])[CH2:23][CH2:22]2)=[CH:18][CH:17]=1.FC1C=CC(CC2CCNCC2)=CC=1>>[CH2:20]([CH:21]1[CH2:26][CH2:25][N:24]([CH2:27][CH2:28][C:29]([C:31]2[CH:40]=[CH:39][C:34]3[NH:35][C:36](=[O:37])[NH:10][C:33]=3[CH:32]=2)=[O:30])[CH2:23][CH2:22]1)[C:19]1[CH:41]=[CH:42][CH:16]=[CH:17][CH:18]=1

Participants

3

Procedure

from 6-(3-chloro-1-oxopropyl)-2,3-dihydrobenzoxazole and 4-(4-fluorobenzyl)piperidine 6-{3-[4-(4-fluorobenzyl)-1-piperidyl]-1-oxopropyl}-2,3-dihydrobenzoxazol-2-one, m.p. 168°-173° C.

Sources & evidence

ORD record
ord-ffe1ce3f5f48484fa317ad0e5f2b908a
Source dataset
uspto-grants-1997_12
Patent number
US05698553

Reaction notes

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