Acetone → HCID 46195425, compound

HRID 2385249Notes

Reaction equation

HRID 2385249 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]2([C:18]3[C:13](=[CH:14][C:15]4[O:21][CH2:20][CH2:19][C:16]=4[CH:17]=3)[O:12][CH2:11][CH2:10]2)[C:2]1=[O:22].CC(C)=O.Br[CH2:28][C:29]1[O:30][C:31]([C:34]([F:37])([F:36])[F:35])=[CH:32][CH:33]=1.BrCC1CCCCO1>CC(=O)CC>[F:35][C:34]([F:37])([F:36])[C:31]1[O:30][C:29]([CH2:28][N:1]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[C:3]3([C:18]4[C:13](=[CH:14][C:15]5[O:21][CH2:20][CH2:19][C:16]=5[CH:17]=4)[O:12][CH2:11][CH2:10]3)[C:2]2=[O:22])=[CH:33][CH:32]=1

Participants

6

Procedure

Following the procedure as described in EXAMPLE 4 and making non-critical variations using 2,3,6,7-tetrahydrospiro[furo[3,2-g]chromene-5,3′-indol]-2′(1′H)-one to replace 5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-2″(1′H)-one, acetone to replace butanone, and 2-(bromomethyl)-5-(trifluoromethyl)furan to replace 2-(bromomethyl)tetrahydro-2H-pyran, 1′-{[5-(trifluoromethyl)furan-2-yl]methyl}-2,3,6,7-tetrahydrospiro[furo[3,2-g]chromene-5,3′-indol]-2′(1′H)-one was obtained (43%) as a colorless solid: 1H NMR (300 MHz, CDCl3) δ7.36-6.93 (m, 4H), 6.76-6.70 (m, 1H), 6.38 (d, J=3.5 Hz, 1H), 6.36 (s, 1H), 6.21 (s, 1H), 4.98 (ABq, 2H), 4.80-4.69 (m, 1H), 4.45 (t, J=8.6 Hz, 2H), 4.36-4.28 (m, 1H), 2.92 (t, J=8.5 Hz, 2H), 2.23-2.16 (m, 2H); 13C NMR (75 MHz, CDCl3) δ179.3, 160.6, 155.5, 152.2, 152.1, 141.8, 141.6, 141.3, 135.2, 128.3, 124.1, 123.5, 123.5, 120.6, 120.4, 117.0, 112.6 (2C), 112.5 (2C), 112.1, 109.1, 108.6, 98.6, 71.8, 62.0, 47.8, 36.7, 32.4, 28.8; MS (ES+) m/z 441.7 (M+1).

Sources & evidence

ORD record
ord-55d1975a7ec64195a43dcc4c4e7ab0ca
Source dataset
uspto-grants-2012_09
Patent number
US08263606B2

Reaction notes

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