Hydrochloric Acid → HCID 66746081, compound

HRID 2169980Notes

Reaction equation

HRID 2169980 reaction equation
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[O:12][CH2:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)[N:5]=[C:4]([CH3:19])[C:3]=1[C:20]([OH:22])=[O:21].[ClH:23]>>[ClH:23].[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[O:12][CH2:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)[N:5]=[C:4]([CH3:19])[C:3]=1[C:20]([OH:22])=[O:21]

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 545884934-Amino-5-(cyclopentylmethoxy)-2-methylquinoline-3-carboxylic acid

Product 1

HCID 66746081HCID 66746081, compound

Procedure

Prepared as in Example 123 from 4-amino-5-(cyclopentylmethoxy)-2-methylquinoline-3-carboxylic acid (Example 18) as a white solid (100%). 1H NR (400 MHz, DMSO-d6) δ 1.29-1.37 (m, 2H), 1.51-1.66 (m, 4H), 1.82-1.90 (m, 2H), 2.43-2.51 (m, 1H), 2.81 (s, 3H), 4.18 (d, J=7.2 Hz, 2H), 7.24 (d, J=8.4 Hz, 1H), 7.60 (d, J=8.4 Hz, 1H), 7.84 (t, J=8.4 Hz, 1H), 9.25 (brs, 1H), 9.86 (brs, 1H). MS 301 (MH+—HCl).

Sources & evidence

ORD record
ord-751292ddefdd406aa7c788db66caedc6
Source dataset
uspto-grants-2015_06
Patent number
US09049878B2

Reaction notes

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