Methylamine → HCID 178466711, compound

HRID 2083051Notes

Reaction equation

HRID 2083051 reaction equation
[CH3:1][NH2:2].[C:3]([NH:5][C:6](=[N:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[C:19]([O:20][CH2:21][CH3:22])=[CH:18][CH:17]=[CH:16][N:15]=1)SC)#[N:4]>C(O)C>[C:3]([NH:5][C:6]([NH:2][CH3:1])=[N:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[C:19]([O:20][CH2:21][CH3:22])=[CH:18][CH:17]=[CH:16][N:15]=1)#[N:4]

Participants

4

Reactant 2

HCID 6329MethylamineHCID 20474235N-cyano-N'-[2-((3-ethoxy-2-pyridyl)methylthio)ethyl]-S-methylisothiourea

Product 1

HCID 178466711HCID 178466711, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

Methylamine in ethanol (33%, 10 cc) was added to a stirred suspension of N-cyano-N'-[2-((3-ethoxy-2-pyridyl)methylthio)ethyl]-S-methylisothiourea (1.0 g) in ethanol (5 cc) and the mixture was left to stand overnight. Nitrogen was bubbled through the solution for one hour and the solution was concentrated and crystals which deposited were filtered off and recrystallised from ethanol/ether to give the title product (0.7 g) m.p. 126.5°-127.5°.

Workup

  1. waitthe mixture was left
  2. customNitrogen was bubbled through the solution for one hour
  3. concentrationthe solution was concentrated
  4. filtrationcrystals which deposited were filtered off
  5. customrecrystallised from ethanol/ether

Sources & evidence

ORD record
ord-23cc5437f0d2452eb05d4bc193a2eccb
Source dataset
uspto-grants-1978_04
Patent number
US04083983

Reaction notes

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