Piperidine → HCID 23435934, compound

HRID 2120900Notes

Reaction equation

[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[C:14]([Br:29])[C:15]2[CH:20]=[CH:19][C:18]([C:21]([N:23]3[CH2:28][CH2:27]O[CH2:25][CH2:24]3)=[O:22])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].N1CCCC[CH2:31]1>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[C:14]([Br:29])[C:15]2[CH:20]=[CH:19][C:18]([C:21]([N:23]3[CH2:24][CH2:25][CH2:31][CH2:27][CH2:28]3)=[O:22])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

Reactant 2

HCID 8082Piperidine

HCID 23435899HCID 23435899, compound

Product 1

HCID 23435934HCID 23435934, compound

Procedure

Same procedure as described for the preparation of compound 82, but using piperidine in place of morpholine.

Sources & evidence

ORD record: ord-f1aea4f055d347f5840762f78712b12c
Source dataset: uspto-grants-2004_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06693117B2

Reaction notes

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