Sodium Hydroxide → HCID 59997317, compound

HRID 1815587Notes

Reaction equation

HRID 1815587 reaction equation
[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]([CH2:19][C@H:20]3[O:24]C(C)(C)[N:22]([C:27]([O:29][C@@H:30]4[C@H:37]5[C@H:33]([O:34][CH2:35][CH2:36]5)[O:32][CH2:31]4)=[O:28])[C@H:21]3[CH2:38][C:39]3[CH:44]=[CH:43][C:42]([O:45][CH2:46][C:47]4[CH:52]=[CH:51][CH:50]=[CH:49][N:48]=4)=[CH:41][CH:40]=3)[CH2:15][CH:16]([CH3:18])[CH3:17])(=[O:13])=[O:12])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.[OH-].[Na+]>C(O)(C)C.Cl>[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([S:11]([N:14]([CH2:15][CH:16]([CH3:18])[CH3:17])[CH2:19][C@@H:20]([OH:24])[C@@H:21]([NH:22][C:27](=[O:28])[O:29][C@@H:30]3[C@H:37]4[C@H:33]([O:34][CH2:35][CH2:36]4)[O:32][CH2:31]3)[CH2:38][C:39]3[CH:40]=[CH:41][C:42]([O:45][CH2:46][C:47]4[CH:52]=[CH:51][CH:50]=[CH:49][N:48]=4)=[CH:43][CH:44]=3)(=[O:13])=[O:12])=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1

Participants

5

Procedure

70 mg of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl (4S,5R)-5-{[(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)(isobutyl)amino]methyl}-2,2-dimethyl-4-[4-(2-pyridinylmethoxy)benzyl]-1,3-oxazolidine-3-carboxylate were dissolved in 15 mL of isopropanol and 5 mL of concentrated hydrochloric acid. After 2 h, the reaction was treated with excess 3N sodium hydroxide and extracted with ethyl acetate. Evaporation of the solvent gave 67 mg of the desired product. 1H NMR: 0.83(6H,dd), 1.4-1.8(4H,m), 2.6-3.2(7H,m), 3.6(2H,m), 3.75(2H,m), 3.9(2H,m), 4.25(4H,bs), 4.95(1H,d), 5.0(1H,m), 5.6(1H,d), 6.9(2H,d), 6.95(2H,d), 7.1(2H,d), 7.2(2H,m), 7.45(1H,d), 7.7(1H,t), 8.58(1H,d).

Workup

  1. extractionextracted with ethyl acetate
  2. customEvaporation of the solvent

Sources & evidence

ORD record
ord-84465f3ddbf147d1ad011d4783a00d9c
Source dataset
uspto-grants-2005_04
Patent number
US06878728B1

Reaction notes

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