Hydrochloric Acid → HCID 67319103, compound

HRID 2378636Notes

Reaction equation

HRID 2378636 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH:14]2[C:19](=[O:20])[C:18]3[CH:21]=[CH:22][CH:23]=[CH:24][C:17]=3[NH:16][S:15]2(=[O:26])=[O:25])[CH2:10][CH2:9]1)=O)(C)(C)C.O1CCOCC1.[ClH:33]>>[ClH:33].[O:26]=[S:15]1(=[O:25])[CH:14]([CH:11]2[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[C:19](=[O:20])[C:18]2[CH:21]=[CH:22][CH:23]=[CH:24][C:17]=2[NH:16]1

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 59731969HCID 59731969, compound

Product 1

HCID 67319103HCID 67319103, compound

Procedure

4-(2,2,4-Trioxo-1,2,3,4-tetrahydro-2,1-benzothiazin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (175 mg, 0.46 mmol) was dissolved in 4M hydrogen chloride in 1,4-dioxane (3.0 mL, 12.0 mmol). Reaction stirred at room temperature for 45 minutes. Reaction mixture was concentrated to dryness in vacuo. Title compound was obtained as pink solid in quantitative yield. MS m/e (M+H)+=281.1.

Workup

  1. customReaction
  2. customReaction mixture
  3. concentrationwas concentrated to dryness in vacuo

Sources & evidence

ORD record
ord-2e2078bbe2984a78867b4f3307ec13e1
Source dataset
uspto-grants-2008_12
Patent number
US07470679B2

Reaction notes

Loading…