Dimethylformamide dimethyl acetal → HCID 21905833, compound
Reaction equation
[CH3:1]OC(OC)N(C)C.[CH:9]([N:22]1[CH2:25][C:24]([NH:29][CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)([C:26]([NH2:28])=[O:27])[CH2:23]1)([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[CH:9]([N:22]1[CH2:23][C:24]2([C:26](=[O:27])[N:28]=[CH:1][N:29]2[CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH2:25]1)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
3
Procedure
N,N-Dimethylformamide dimethyl acetal (16 ml, 121 mmol) was combined with 1-benzhydryl-3-benzylaminoazetidine-3-carboxylic acid amide (I-(13A-9)b; 3.03 g, 8.16 mmol) and heated to reflux. After 4 hours, the suspension was cooled and extracted from saturated aqueous NaHCO3 with ethyl acetate. The combined extracts were dried (Na2SO4), and concentrated, in vacuo, to the crude solid (3.50 g). Purification of the residue on a Biotage™ Flash 40M column using 0–3% methanol in methylene chloride as eluant afforded I-(29A-6)a as a yellowish solid (1.92 g, 62%): +ES MS (M+1) 382.3; 1H NMR (400 MHz, CD3OD) δ 8.66 (s, 1H), 7.59 (d, J=7.1 Hz, 2H), 7.49–7.11 (m, 13H), 5.12 (s, 2H), 4.44 (s, 1H), 3.31 (d, J=9.6 Hz, 2H), 3.20 (d, J=9.6 Hz, 2H).
Workup
- temperatureheated to reflux
- temperaturethe suspension was cooled
- extractionextracted from saturated aqueous NaHCO3 with ethyl acetate
- dry with materialThe combined extracts were dried (Na2SO4)
- concentrationconcentrated, in vacuo, to the crude solid (3.50 g)
- customPurification of the residue on a Biotage™ Flash 40M column
Sources & evidence
- ORD record
- ord-3c265ec7698646edaa74616cbba7532a
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07129239B2
Reaction notes
Loading…