1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 58562579, compound

HRID 2175525Notes

Reaction equation

HRID 2175525 reaction equation
[CH2:1]([O:8][C:9]([N:11]([C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26]([F:29])([F:28])[F:27])[CH:24]=2)[N:19]=[CH:18][CH:17]=1)[CH2:12][C:13]([OH:15])=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCN=C=NCCCN(C)C.[NH2:41][CH:42]1[CH2:45][N:44]([C:46]([O:48][C:49]([CH3:52])([CH3:51])[CH3:50])=[O:47])[CH2:43]1.C1C=CC2N(O)N=NC=2C=1.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[CH2:1]([O:8][C:9]([N:11]([C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26]([F:29])([F:28])[F:27])[CH:24]=2)[N:19]=[CH:18][CH:17]=1)[CH2:12][C:13]([NH:41][CH:42]1[CH2:43][N:44]([C:46]([O:48][C:49]([CH3:52])([CH3:51])[CH3:50])=[O:47])[CH2:45]1)=[O:15])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

7

Procedure

A solution of 2-(((benzyloxy)carbonyl)(6-(trifluoromethyl)quinolin-4-yl)amino)acetic acid (306 mg, 0.757 mmol, prepared in step F) and EDCI (217 mg, 1.13 mmol) in DCM (10 mL) was stirred until a clear solution resulted. This solution was added to a suspension of tert-butyl 3-aminoazetidine-1-carboxylate (156 mg, 0.908 mmol) and HOBt (116 mg, 0.757 mmol) in DCM (10 mL). The reaction mixture was stirred overnight at ambient temperature and poured onto saturated aqueous sodium bicarbonate, extracting with ethyl acetate. Concentration of the organic layer followed by purification of the residue by flash chromatopgraphy (silica gel, 0-20% MeOH/ethyl acetate) afforded the product.

Workup

  1. customresulted
  2. extractionextracting with ethyl acetate
  3. customConcentration of the organic layer followed by purification of the residue by flash chromatopgraphy (silica gel, 0-20% MeOH/ethyl acetate)
  4. customafforded the product

Sources & evidence

ORD record
ord-c34e92342d5d43aea25ab1643804c378
Source dataset
uspto-grants-2015_06
Patent number
US09062048B2

Reaction notes

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