Diisopropylethylamine → 4-{3-[4-(2,3-Dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)piperazin-1-yl]propyl}-6-methoxy-2H-1,4-benzoxazin-3(4H)-one

HRID 1644405Notes

Reaction equation

HRID 1644405 reaction equation
FC(F)(F)[C:3](O)=[O:4].[CH3:8][O:9][C:10]1[CH:29]=[CH:28][C:13]2CO[C:16](=[O:27])[N:17]([CH2:18][CH2:19][CH2:20][N:21]3[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]3)[C:12]=2[CH:11]=1.C(N(CC)C(C)C)(C)C.[O:39]1[C:48]2[CH:47]=[C:46]([CH:49]=O)[N:45]=[CH:44][C:43]=2[O:42][CH2:41][CH2:40]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl.CO>[O:39]1[C:48]2[CH:47]=[C:46]([CH2:49][N:24]3[CH2:23][CH2:22][N:21]([CH2:20][CH2:19][CH2:18][N:17]4[C:12]5[CH:11]=[C:10]([O:9][CH3:8])[CH:29]=[CH:28][C:13]=5[O:4][CH2:3][C:16]4=[O:27])[CH2:26][CH2:25]3)[N:45]=[CH:44][C:43]=2[O:42][CH2:41][CH2:40]1

Participants

6

Procedure

7-Methoxy-1-(3-piperazin-1-ylpropyl)-1,4-dihydro-2H-3,1-benzoxazin-2-one trifluoroacetate (Intermediate 118, crude, 963 mg, 1.81 mmol) was converted to the free base with N,N-diisopropylethylamine and reacted with 2,3-dihydro[1,4]dioxino[2,3-c]pyridine-7-carbaldehyde (WO 2004/058144) (203 mg, 123 mmol) and sodium triacetoxy borohydride (240 mg, 1.10 mmol) as described for Example 55 to give the free base of the product as an oil after chromatography on silica gel with dichloromethane/methanol (93:7), 125 mg (22%).

Sources & evidence

ORD record
ord-d85816b47de24178834f38facb3a9585
Source dataset
uspto-grants-2012_02
Patent number
US08124602B2

Reaction notes

Loading…