Hydrochloric Acid → ({[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]carbonyl}amino)acetic acid

HRID 17206Notes

Reaction equation

[NH2:1][C:2]1[C:7]2[C:8]([C:11]3[CH:16]=[CH:15][C:14]([NH:17][C:18]([C:20]4[N:21]([CH3:29])[C:22]5[C:27]([CH:28]=4)=[CH:26][CH:25]=[CH:24][CH:23]=5)=[O:19])=[C:13]([O:30][CH3:31])[CH:12]=3)=[CH:9][S:10][C:6]=2[C:5]([C:32]([NH:34][CH2:35][C:36]([O:38]C)=[O:37])=[O:33])=[CH:4][N:3]=1.[OH-].[Na+].O.Cl>O1CCOCC1>[NH2:1][C:2]1[C:7]2[C:8]([C:11]3[CH:16]=[CH:15][C:14]([NH:17][C:18]([C:20]4[N:21]([CH3:29])[C:22]5[C:27]([CH:28]=4)=[CH:26][CH:25]=[CH:24][CH:23]=5)=[O:19])=[C:13]([O:30][CH3:31])[CH:12]=3)=[CH:9][S:10][C:6]=2[C:5]([C:32]([NH:34][CH2:35][C:36]([OH:38])=[O:37])=[O:33])=[CH:4][N:3]=1

Participants

Conditions

Temperature: 50 °C

Procedure

To a mixture of methyl ({[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]carbonyl}amino)acetate (0.130 g, 0.239 mmol) in 1,4 dioxane (10 mL) was added 2M sodium hydroxide in water (0.260 mL, 0.521 mmol). The resulting solution was heated at 50° C. for 3 hours. 1M hydrochloric acid was added until pH of the mixture was 4 and solvent was removed under reduced pressure. The resulting white solid was washed with water (2 mL) and filtered and dried to furnish the title compound (64 mg, 0.121 mmol): LCMS (Conditions b): MH+=530 RT=2.03 min; 1H NMR (DMSO-d6, 400 MHz) δ 12.65 (1 H), 9.50 (1 H), 8.95 (1 H), 8.60 (1 H), 8.02 (1 H), 7.71 (2 H), 7.58 (1 H), 7.35 (2 H), 7.21 (1 H), 7.15 (1 H), 7.09 (1 H), 6.29 (2 H), 4.04 (3 H), 3.97 (2 H), 3.92 (3 H).

Workup

customwas removed under reduced pressure
washThe resulting white solid was washed with water (2 mL)
filtrationfiltered
customdried

Sources & evidence

ORD record: ord-13ac0b3dbe9b433bbd3dd2236c899c80
Source dataset: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07737160B2

Reaction notes

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