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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647591Generated: October 29, 2026

Dimethylcarbamoyl Chloride → N,N-Dimethyl-N'-[(1,3,4,9-tetrahydro-1-methylpyrano[3,4-b]indol-1-yl)methyl]-urea

https://huagongshe.com/reaction/647591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1,3,4,9-Tetrahydro-1-methylpyrano[3,4-b]indol-1-methanamineHCID 12708181—
SolventDiethyl EtherHCID 3283—
ProductN,N-Dimethyl-N'-[(1,3,4,9-tetrahydro-1-methylpyrano[3,4-b]indol-1-yl)methyl]-ureaHCID 1270819485.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

Dimethylcarbamic chloride (3.95 g) is added to a solution at 0° C. of 1,3,4,9-tetrahydro-1-methylpyrano[3,4-b]indole-1-methanamine (7.9 g, described in Example 3), triethylamine (3.7 g) and tetrahydrofuran (200 ml) over a period of 5 minutes. The mixture is stirred at 0° to 5° C. for 30 minutes and at 25° C. for 18 hours. Diethyl ether (200 ml) is added, the mixture is filtered and the filtrate is evaporated. The residue is crystallized from diethyl ether to obtain the title compound (9.0 g); mp 153°-155° C.; ir (CHCl3) 3450-3250 and 1635 cm-1 ; nmr(CDCl3) δ1.51(s) and 2.69(m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409224
Source datasetuspto-grants-1983_10
ORD IDord-dd4c25acff1d4716aaa5e2953ab4c3ed
Source noteuspto-grants-1983_10