(1-Isopropylpiperidin-4-yl)methanamine → HCID 44331553, compound

HRID 1634751Notes

Reaction equation

HRID 1634751 reaction equation
[O:1]1[CH2:3][C@H:2]1[CH2:4][O:5][C:6]1[C:18]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]=2[CH:9]=[CH:8][CH:7]=1.[NH2:19][CH2:20][CH:21]1[CH2:26][CH2:25][N:24]([CH:27]([CH3:29])[CH3:28])[CH2:23][CH2:22]1>>[CH:9]1[C:10]2[NH:11][C:12]3[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=3)[C:18]=2[C:6]([O:5][CH2:4][C@@H:2]([OH:1])[CH2:3][NH:19][CH2:20][CH:21]2[CH2:26][CH2:25][N:24]([CH:27]([CH3:29])[CH3:28])[CH2:23][CH2:22]2)=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 7258859(1-Isopropylpiperidin-4-yl)methanamineHCID 10879208(S)-(+)-4-(2,3-Epoxypropoxy)carbazole

Product 1

HCID 44331553HCID 44331553, compoundYield 34.1%

Procedure

Prepared from 4-[(2S)-oxiranylmethoxy]-9H-carbazole (0.239 g, 1.0 mmol) and 4-aminomethyl-1-isopropylpiperidine (0.312 g, 2.0 mmol) of according to the procedure used for Example 2 to give 0.135 g of the title compound as a white solid.

Sources & evidence

ORD record
ord-6bf32bb37ada4bcbb936277af47481f0
Source dataset
uspto-grants-2003_01
Patent number
US06506901B2

Reaction notes

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