1,2-Dichloroethane → HCID 22135636, compound

HRID 1827127Notes

Reaction equation

HRID 1827127 reaction equation
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][CH:14]([C:17]([OH:19])=O)[CH2:13][CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:20][C:21]1[C:26]([CH3:27])=[CH:25][CH:24]=[CH:23][N:22]=1.C(Cl)CCl.C1C=NC2N(O)N=NC=2C=1>CN(C=O)C>[CH3:27][C:26]1[C:21]([NH:20][C:17]([CH:14]2[CH2:13][CH2:12][N:11]([C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[O:10])[CH2:16][CH2:15]2)=[O:19])=[N:22][CH:23]=[CH:24][CH:25]=1

Participants

6

Reactant 4

HCID 111,2-DichloroethaneHCID 153472-Amino-3-methylpyridineHCID 181649HOAtHCID 7364891-Carbobenzoxy-4-piperidinecarboxylic Acid

Product 1

HCID 22135636HCID 22135636, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

The benzyl 4-{[(3-methyl-2-pyridinyl)amino]carbonyl}-1-piperidinecarboxylate was prepared as described in EXAMPLE 1, except that 1-[(benzyloxy)carbonyl]-4-piperidinecarboxylic acid (5.00 g, 18.99 mmol), 2-amino-3-methylpyridine (2.16 g, 19.94 mmol), EDC (4.37 g, 22.79 mmol), and HOAt (2.71 g, 19.94 mmol) and DMF (3 mL) were used as starting materials. Benzyl 4-{[(3-methyl-2-pyridinyl)amino]carbonyl}-1-piperidinecarboxylate was isolated as an off-white solid and used without further purification.

Workup

  1. customThe benzyl 4-{[(3-methyl-2-pyridinyl)amino]carbonyl}-1-piperidinecarboxylate was prepared

Sources & evidence

ORD record
ord-074d7cdccad94a8aa03d5f14d5dc44ad
Source dataset
uspto-grants-2006_05
Patent number
US07053089B2

Reaction notes

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