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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545585Generated: October 29, 2026

O-Methylhydroxylamine hydrochloride → HCID 86638398, compound

https://huagongshe.com/reaction/545585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 59161293HCID 59161293—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 86638398HCID 8663839862%

Reaction Conditions

Temperature25 °C

Reaction Steps

Dissolve (R)-N-[6-formyl-9-(2-methyl-thiazol-4-ylmethyl)-2,3,4,9-tetrahydro-1H-carbazol-3-yl]-isobutyramide (Example 211) (53 mg, 0.13 mmol) and methoxyamine HCl (22 mg, 0.27 mmol) in pyridine (1 mL). Stir the reaction mixture for 18 h at 25° C. Dilute the reaction mixture with water (2 mL), 1N HCl (1 mL), and EtOAc (10 mL). Load the mixture onto a Varian ChemElut CE1005 solid-phase extraction cartridge (Varian part number 12198006), then elute, collect, and concentrate 50 mL EtOAc to give the crude product (59 mg) as a white solid. Purify on 8 g silica gel (50-60% EtOAc/hexanes) to afford 34 mg (62%) of the title compound as a white solid. MS (ES): m/z 425 (M+1), 469 (M+HCO2−); 1H NMR (CDCl3): δ 8.16 (s, 1H), 7.63 (d, 1H, J=1.3 Hz), 7.44 (dd, 1H, J=8.6, 1.5 Hz), 7.24 (d, 1H, J=8.5 Hz), 6.36 (s, 1H), 5.55 (d, 1H, J=7.9 Hz), 5.29 (td, 2H, J=24.7, 9.0 Hz), 4.41 (m, 1H), 3.96 (s, 3H), 3.13 (dd, 1H, J=15.4, 4.8 Hz), 2.80 (m, 2H), 2.68 (s, 3H), 2.62 (dd, 1H, J=15.6, 6.8 Hz), 2.30 (m, 1H), 2.14-1.97 (m, 2H), 1.14 (d, 6H, J=6.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935722B2
Source datasetuspto-grants-2011_05
ORD IDord-6887b333e079499a9de250e7a7d0492f
Source noteuspto-grants-2011_05