1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 69421660, compound

HRID 1272922Notes

Reaction equation

HRID 1272922 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14](C#N)[CH:15]=3)[N:10]([CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][O:20]3)[N:9]=2)[CH:5]=[CH:6][CH:7]=1.[C:25]([O:28][C@@H:29]([CH3:33])[C:30](O)=[O:31])(=[O:27])[CH3:26].Cl.[CH3:35][N:36](C)CCCN=C=NCC>ClCCl>[C:25]([O:28][C@H:29]([C:30](=[O:31])[NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10]([CH:19]3[CH2:24][CH2:23][CH:22]([C:35]#[N:36])[CH2:21][O:20]3)[N:9]=2)[CH:3]=1)[CH3:33])(=[O:27])[CH3:26]

Participants

5

Reactant 3

HCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride2×HCID 6326324(2S)-2-(Acetyloxy)propanoic acidHCID 22480146HCID 22480146, compound

Product 1

HCID 69421660HCID 69421660, compoundYield 85%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 3-(3-aminophenyl)-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carbonitrile (0.400 g, 1.25 mmol) in dichloromethane (50 mL), was added (S)-(−)-2-acetoxy propionic acid (0.128 mL, 1.38 mmol) and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (EDCI) (0.287 g, 1.5 mmol). After overnight reaction at room temperature, 0.6 equivalent of carboxylic acid and EDCI were added. After 12 hours at room temperature, the reaction was complete. The reaction mixture was partitioned between dichloromethane and water. The organic phase was dried under vacuum and the title product was used in the subsequent step without further purification (0.460 g, 85% yield): ES-MS (m/z) 433 [M+H]+.

Workup

  1. customAfter overnight reaction at room temperature
  2. customThe reaction mixture was partitioned between dichloromethane and water
  3. customThe organic phase was dried under vacuum
  4. customthe title product was used in the subsequent step without further purification (0.460 g, 85% yield)

Sources & evidence

ORD record
ord-48eb09291c1949aabeb73c283f3c72c8
Source dataset
uspto-grants-2007_04
Patent number
US07208513B2

Reaction notes

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