Diisopropylethylamine → HCID 178465356, compound

HRID 353973Notes

Reaction equation

HRID 353973 reaction equation
[CH2:1]([NH:3][C:4]([N:6]=[C:7](OC)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:5])[CH3:2].Cl.Cl.[NH2:18][CH:19]([CH2:32][CH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1)[C:20]([NH:22][C:23]1([C:30]#[N:31])[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]1)=[O:21].C(N(CC)C(C)C)(C)C>CO>[C:30]([C:23]1([NH:22][C:20](=[O:21])[CH:19]([NH:18][C:7](=[N:6][C:4](=[O:5])[NH:3][CH2:1][CH3:2])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:32][CH:33]2[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]2)[CH2:24][CH2:25][N:26]([CH3:29])[CH2:27][CH2:28]1)#[N:31]

Participants

5

Procedure

A solution of 1-ethyl-3-(methoxy-phenyl-methylene)-urea (350 mg, 1.70 mmol), 2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamide bis hydrochloride salt (512 mg, 1.40 mmol) and N,N-diisopropylethylamine (352 mg, 2.73 mmol) in dry methanol (5.0 mL) was stirred at room temperature for 60 h. The reaction mixture was concentrated and the resulting residue was chromatographed over 50 g of flash silica gel using dichloromethane to 5% methanol in dichloromethane as the eluant. This provided the desired product as a light yellow solid (280 mg, 43%) which was further purified by HPLC using a 20×250 mm C18 reverse phase column with the method being 20% acetonitrile in water to 90% acetonitrile in water. MS, m/z 467=M+1.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customthe resulting residue was chromatographed over 50 g of flash silica gel

Sources & evidence

ORD record
ord-3cdbeef18acc4ea2a87d1e33d6490e40
Source dataset
uspto-grants-2004_06
Patent number
US06756372B2

Reaction notes

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