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Sodium Methoxide → HCID 86697864, compound

HRID 571628
Notes
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Reaction equation

HRID 571628 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:14][CH2:13][C:12]2[S:15][C:16](Br)=[N:17][C:11]=2[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:19][O-:20].[Na+]>CO>[C:1]([O:5][C:6]([N:8]1[CH2:14][CH2:13][C:12]2[S:15][C:16]([O:20][CH3:19])=[N:17][C:11]=2[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 10942334Sodium MethoxideHCID 71651202tert-butyl 2-bromo-4H,5H,6H,7H,8H-(1,3)thiazolo(4,5-d)azepine-6-carboxylate

Product 1

HCID 86697864HCID 86697864, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

1.00 g (3.00 mmol) bromo-4,5,7,8-tetrahydro-thiazolo[4,5-d]azepine-6-carboxylic acid tert-butyl ester, 0.40 g (7.00 mmol) sodium methylate in 15 mL methanol were heated at 100° C. for 4 h under microwave irradiation. The mixture was purified by chromatography.

Workup

  1. customThe mixture was purified by chromatography

Sources & evidence

ORD record
ord-e0578dacedec4d328ea8746c99d34f47
Source dataset
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09029360B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes