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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962876Generated: October 30, 2026

Methanol → HCID 131719933, compound

https://huagongshe.com/reaction/962876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl iodideHCID 6328—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 19610500HCID 19610500—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductHCID 131719933HCID 13171993393.9%

Reaction Steps

In a similar manner to Example 12, methyl 4-[2-methyl-3-(4-thio-carbamoylbenzoyl) carbazoyl]phenoxyacetate (2.5 g) was reacted with iodomethane (15 ml) in acetone (150 ml) and the resultant product was treated with ammonium acetate (6.5 g), methanol (100 ml) and dichloromethane (100 ml). This yielded a crude yellow solid, which was triturated with methanol, collected and washed with methanol/dichloromethane, rather than crystallised, to give the title compound (1.3 g) as an off-white solid; m.p. 210° C. (decomposes); NMR Spectrum (DMSO--d6) 1.73 (3H, s), 3.20 (3H, s), 3.55 (3H, s), 4.76 (2H, s), 6.90 (2H, d), 7.53 (2H, d), 7.80 (4H, m), 8.50-11.0 (2H, br s); Mass Spectrum m/Z 385 (M+H)+ ; Elemental Analysis: calculated for C19H20N4O5. 1.0 CH3CO2H. 0.8 H2O: C, 55.0%; H, 5.6%; N, 12.2%; found: C, 55.0%; H, 5.4%; N, 11.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760057
Source datasetuspto-grants-1998_06
ORD IDord-b42a050bd35d4f4990ba9964c4f46e1d
Source noteuspto-grants-1998_06