Hydrochloric Acid → HCID 67667059, compound

HRID 1289994Notes

Reaction equation

HRID 1289994 reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH2:8][CH:7]([NH:10][CH2:11][C:12]2[CH:17]=[C:16]([C:18]3[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=3)[CH:15]=[CH:14][C:13]=2[O:24][CH3:25])[CH:6]1[C:26]1[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=1)=[O:4].[ClH:33]>CO.C(OCC)C>[ClH:33].[ClH:33].[CH3:1][O:2][C:3]([CH:5]1[CH2:9][CH2:8][CH:7]([NH:10][CH2:11][C:12]2[CH:17]=[C:16]([C:18]3[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=3)[CH:15]=[CH:14][C:13]=2[O:24][CH3:25])[CH:6]1[C:26]1[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=1)=[O:4]

Participants

4

Procedure

Exposure of the product from Step B above to 2.2 equivalents of HCl in methanol/ethyl ether followed by evaporation provided the title compound. NMR (400 MHz, CD3OD): δ 9.15 (d, 1H, J=2 Hz), 8.85 (dt, 1H, J=8,2 Hz), 8.80 (d, 1H, J=5 Hz), 8.04 (dd, 1H, J=8,5 Hz), 7.92 (dd, 1H, J=9,2 Hz), 7.82 (d, 1H, J=2 Hz), 7.43 (dd, 2H, J=9,5 Hz), 7.26 (d, 1H, J=9 Hz), 7.21 (t, 2H, J=9 Hz), 4.30 (d, 1H, J=13 Hz), 4.14 (d, 1H, J=13 Hz), 3.99-3.92 (m, 1H), 3.90 (dd, 1H, J=9,8 Hz), 3.80 (s, 3H), 3.63 (s, 3H), 3.42 (quartet, 1H, J=8 Hz), 2.52-2.38 (m, 2H), 2.22-2.12 (m, 1H), 2.07-1.96 (m, 1H).

Sources & evidence

ORD record
ord-11a7c6d660774581a46a7ee1755933a1
Source dataset
uspto-grants-1998_05
Patent number
US05750549

Reaction notes

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