Dichloromethane → HCID 9894801, compound

HRID 1061232Notes

Reaction equation

HRID 1061232 reaction equation
C([O:5][C:6](=[O:44])[CH2:7][N:8]1[C:12](=[O:13])[CH:11]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][CH:24]([NH:27][CH2:28][C@H:29]([OH:42])[C:30]4[CH:35]=[CH:34][C:33]([OH:36])=[C:32]([NH:37][S:38]([CH3:41])(=[O:40])=[O:39])[CH:31]=4)[CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[S:10][C:9]1=[O:43])(C)(C)C.ClCCl.FC(F)(F)C(O)=O>C(OCC)C>[OH:42][C@H:29]([C:30]1[CH:35]=[CH:34][C:33]([OH:36])=[C:32]([NH:37][S:38]([CH3:41])(=[O:39])=[O:40])[CH:31]=1)[CH2:28][NH:27][CH:24]1[CH2:25][CH2:26][N:21]([C:18]2[CH:17]=[CH:16][C:15]([CH2:14][CH:11]3[S:10][C:9](=[O:43])[N:8]([CH2:7][C:6]([OH:44])=[O:5])[C:12]3=[O:13])=[CH:20][CH:19]=2)[CH2:22][CH2:23]1

Participants

5

Procedure

A mixture of 5-[[4-[4-[[(R)-2-hydroxy-2-[4-hydroxy-3-[(methylsulfonyl)amino]-phenyl]ethyl]amino]-1-piperidineyl]phenyl]methyl]-2,4-dioxo-3-thiazolidineacetic acid tert-butyl-ester (300 mg, 0.46 mmol) (which was obtained in Example 64), dichloromethane (5 mL), and trifluoroacetic acid (0.5 mL) was stirred at room temperature for 10 hours. The mixture was then poured into ethyl ether (50 mL), and the precipitated solid was filtered and dried to give an off-white solid (189 mg, 58% yield); mp 158-160° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.58-1.66 (m, 2H), 2.02-2.10 (m, 2H), 2.60-2.64 (m, 2H), 2.85-3.04 (m, 4H), 3.16-3.40 (m, 4H), 3.80 (m, 2H), 4.20 (s, 2H), 4.80 (m, 1H), 5.06 (m, 1H), 6.17 (brs, 1H), 6.87-6.91 (m, 3H), 7.05-7.1 (m, 3H), 7.23 (m, 1H), 8.60 (brs, 1H), 8.80 (s, 1H), 9.94 (s, 1H), 13.3 (brs, 1H); MS (ES) m/z: 649 (MH+).

Workup

  1. filtrationthe precipitated solid was filtered
  2. customdried

Sources & evidence

ORD record
ord-46a418820690433693cbb469618f83a1
Source dataset
uspto-grants-2003_02
Patent number
US06525202B2

Reaction notes

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