Hydrochloric Acid → HCID 18705823, compound

HRID 2287856Notes

Reaction equation

HRID 2287856 reaction equation
[CH2:1]([N:4]([CH2:20][CH2:21][CH3:22])[CH:5]1[CH2:13][C:12]2[C:7](=[CH:8][C:9]([C:17]([O-:19])=O)=[C:10]([C:14]([O-:16])=O)[CH:11]=2)[CH2:6]1)[CH2:2][CH3:3].[CH3:23][O:24][C:25]1[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=1[CH2:27][NH2:28].Cl>>[CH2:20]([N:4]([CH2:1][CH2:2][CH3:3])[CH:5]1[CH2:6][C:7]2=[CH:8][C:9]3[C:17](=[O:19])[N:28]([CH2:27][C:26]4[CH:29]=[CH:30][CH:31]=[CH:32][C:25]=4[O:24][CH3:23])[C:14](=[O:16])[C:10]=3[CH:11]=[C:12]2[CH2:13]1)[CH2:21][CH3:22]

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 812922-MethoxybenzylamineHCID 18705881HCID 18705881, compound

Product 1

HCID 18705823HCID 18705823, compound

Procedure

Using procedure 49, 2-(dipropylamino)-2,3-dihydro-1H-indene-5,6-dicarboxylate (92, 0.35 g, 1.0 mmol) was treated with o-methoxybenzylamine (0.18 mL, 1.4 mmol). Purification using silica gel, eluting with 5:1 CH2Cl2 /acetone, afforded an oil that was converted to an HCl salt and recrystallized from hot MeOH/EtOAc to give 103 as a white solid (m.p.205° C.).

Workup

  1. customPurification
  2. washeluting with 5:1 CH2Cl2 /acetone
  3. customafforded an oil that
  4. customrecrystallized from hot MeOH/EtOAc

Sources & evidence

ORD record
ord-9611385f75a24db5aa3100c1355ec7e7
Source dataset
uspto-grants-2000_07
Patent number
US06084130

Reaction notes

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