N-(3-chloropropyl)piperidine hydrochloride → HCID 68139404, compound

HRID 1730933Notes

Reaction equation

HRID 1730933 reaction equation
[C:1]1([C:7]2[C:15]3[C:10](=[CH:11][CH:12]=[C:13]([CH3:16])[CH:14]=3)[NH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[N:18]1([CH2:24][CH2:25][CH2:26][Cl:27])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>>[ClH:27].[N:18]1([CH:24]([C:14]2[C:13]([CH3:16])=[CH:12][CH:11]=[C:10]3[C:15]=2[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[N:8][NH:9]3)[CH2:25][CH3:26])[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1

Participants

3

Reactant 2

HCID 79624N-(3-chloropropyl)piperidine hydrochlorideHCID 6104125-Methyl-3-phenyl-1H-indazole

Product 1

HCID 68139404HCID 68139404, compound

Procedure

By the procedure similar to that described in Example 1, 3-phenyl-5-methylindazole (4.17 g) and piperidinopropyl chloride hydrochloride were treated to obtain 5.0 g of 1-piperidinopropyl-3-phenyl-5-methylindazole hydrochloride (m.p. 222°-223° C).

Workup

  1. additionwere treated

Sources & evidence

ORD record
ord-c2b54ce3b3874e71a518ba2cb59052a8
Source dataset
uspto-grants-1976_11
Patent number
US03994890

Reaction notes

Loading…