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Hydrochloric Acid → (2R,4S)-1-t-butoxycarbonyl-2-(N-t-butoxycarbonyl-N-sulfamoylamino)methyl-4-mercaptopyrrolidine

HRID 1034511
Notes
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Reaction equation

HRID 1034511 reaction equation
C([S:4][C@@H:5]1[CH2:9][N:8]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[C@@H:7]([CH2:17][N:18]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[S:19](=[O:22])(=[O:21])[NH2:20])[CH2:6]1)(=O)C.C[O-].[Na+].C1(C)C=CC=CC=1.Cl>ClCCl.CO.O>[C:13]([O:12][C:10]([N:8]1[CH2:9][C@@H:5]([SH:4])[CH2:6][C@@H:7]1[CH2:17][N:18]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[S:19](=[O:22])(=[O:21])[NH2:20])=[O:11])([CH3:15])([CH3:16])[CH3:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 313Hydrochloric AcidHCID 1140TolueneHCID 10942334Sodium MethoxideHCID 57156698(2R,4S)-4-acetylthio-1-t-butoxycarbonyl-2-(N-t-butoxycarbonyl-N-sulfamoylamino)methylpyrrolidine

Product 1

HCID 10549579(2R,4S)-1-t-butoxycarbonyl-2-(N-t-butoxycarbonyl-N-sulfamoylamino)methyl-4-mercaptopyrrolidine

Reagents, catalysts & solvents

3
HCID 887MethanolSolventHCID 962WaterSolvent2×HCID 6344DichloromethaneSolvent

Procedure

To a solution of (2R,4S)-4-acetylthio-1-t-butoxycarbonyl-2-(N-t-butoxycarbonyl-N-sulfamoylamino)methylpyrrolidine (i.e., a substrate) in dichloromethane, 4.92M sodium methoxide (NaOMe) in methanol is added. The mixture is stirred. The conditions for this reaction are shown in Table 3, Step A-7. The reaction mixture is diluted with water. The water layer is taken, toluene is added thereto, and acidified with conc. hydrochloric acid under ice cooling. The organic layer is taken, successively washed with water and saturated brine, dried over magnesium sulfate, and concentrated in vacuo to give (2R,4S)-1-t-butoxycarbonyl-2-(N-t-butoxycarbonyl-N-sulfamoylamino)methyl-4-mercaptopyrrolidine. mp. 90.0° to 91.5° C. NMR δ(CDCl3) ppm: 1.43(s, 9H), 1.52(s, 9H), 1.72(d, J=7.0 Hz, 1H), 1.9 to 2.0(m, 2H), 3.2 to 3.8(m, 5H), 4.5(m, 1H), 6.11(s, 2H). IR ν (KBr) cm-1 : 3220, 1698, 1683. Elemental Analysis (C15H29O6N3S2) Calcd. C:43.78, H:7.10, N:10.21, S:15.58. Found. C:43.55, H:7.11, N:10.37, S:15.75.

Workup

  1. washsuccessively washed with water and saturated brine
  2. dry with materialdried over magnesium sulfate
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-b5606125951a4dfca90f3d843651779f
Source dataset
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05317016

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes