Triethylamine → HCID 67165929, compound

HRID 510672Notes

Reaction equation

HRID 510672 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][C:14]1[CH:22]=[CH:21][C:17]([C:18](O)=[O:19])=[CH:16][CH:15]=1)[O:9][CH2:8][CH2:7][CH:6]2[C:23]([O:25][CH3:26])=[O:24])#[N:2].Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.O1C2C(=CC=CC=2)CCC1.Cl.[CH3:61][O:62][C:63]1[CH:64]=[C:65]2[C:70](=[CH:71][CH:72]=1)[CH2:69][CH:68]([NH2:73])[CH2:67][CH2:66]2.C(N(CC)CC)C>ClCCCl>[CH3:61][O:62][C:63]1[CH:64]=[C:65]2[C:70](=[CH:71][CH:72]=1)[CH2:69][CH:68]([NH:73][C:18]([C:17]1[CH:16]=[CH:15][C:14]([O:13][C:12]3[CH:11]=[C:10]4[C:5]([CH:6]([C:23]([O:25][CH3:26])=[O:24])[CH2:7][CH2:8][O:9]4)=[CH:4][C:3]=3[C:1]#[N:2])=[CH:22][CH:21]=1)=[O:19])[CH2:67][CH2:66]2

Participants

7

Procedure

A mixture of 4-(6-cyano-4-(methoxycarbonyl)-chroman-7-yloxy)benzoic acid (Preparation 2) (0.0297 g, 0.0841 mmol), 1-(3-(dimethylamino)propyl)-3-ethyl-carbodiimide hydrochloride (0.0177 g, 0.0925 mmol), 1-hydroxybenzotriazole monohydrate (0.0142 g, 0.0925 mmol), and 1,2-dichloroethane (1 ml) was stirred at ambient temperature for 20 minutes. A mixture of chroman-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride (0.0197 g, 0.0924 mmol), triethylamine (0.0585 ml, 0.4203 mmol)), and 1,2-dichloroethane (1 ml) was added to the activated acid and the mixture was stirred for 17 hours at ambient temperature. The crude mixture was purified on silica gel (MeOH in dichloromethane gradient) to provide 29.5 mg of the title compound as a foamy film (69%)

Workup

  1. additionwas added to the activated acid
  2. stirringthe mixture was stirred for 17 hours at ambient temperature
  3. customThe crude mixture was purified on silica gel (MeOH in dichloromethane gradient)

Sources & evidence

ORD record
ord-e4c9cf66d93b4ea6af728897a6e34b33
Source dataset
uspto-grants-2015_08
Patent number
US09096567B2

Reaction notes

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