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Acetyl chloride → HCID 178419001, compound

HRID 7533
Notes
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Reaction equation

HRID 7533 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([NH2:9])[N:3]=1.[CH3:10][O:11][C:12](=[O:16])[CH2:13][N+:14]#[C-:15].[CH:17](=O)[C:18]1[O:22][CH:21]=[CH:20][CH:19]=1.[C:24](Cl)(=[O:26])[CH3:25]>Cl(O)(=O)(=O)=O>[Cl-:8].[C:24]([N+:1]1[C:17]([C:18]2[O:22][CH:21]=[CH:20][CH:19]=2)=[C:15]([NH:14][CH2:13][C:12]([O:11][CH3:10])=[O:16])[N:3]2[C:4]([NH2:9])=[CH:5][C:6]([Cl:8])=[N:7][C:2]=12)(=[O:26])[CH3:25]
ParticipantsProcedureSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6367Acetyl chlorideHCID 7362FurfuralHCID 674322,4-Diamino-6-chloropyrimidineHCID 547815Methyl isocyanoacetate

Product 1

HCID 178419001HCID 178419001, compound

Reagents, catalysts & solvents 1

HCID 24247Perchloric Acid
Solvent

Procedure

Example 27 was carried out in accordance with the general directions for synthesis in process step a) from 1.0 ml (0.1 mmol) 2,6-diamino-4-chloro-pyrimidine (0.1 M, DCM), 0.575 ml (0.115 mmol) isocyanoacetic acid methyl ester solution (0.2 M, DCM), 0.500 ml (0.15 mmol) furfural solution (0.3 M, DCM) and 10 μl perchloric acid (w=20%) and in process step c) and d) by reacting the resultant reaction product with 0.4 mmol acetylchloride.

Sources & evidence

ORD record
ord-e09d80b009c94883976bbcd98164aff7
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07087607B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes